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<h3>Job Description</h3>
Job Description Laboratory Supervisor - Core Lab US-OH-Wilmington Job ID: 2025-57109 Type: Full-Time # of Openings: 1 Category: Laboratory 1500 Rombach Ave Overview 

Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether it’s by providing care in our facilities, training the next generation of health care professionals, or serving others through international outreach.

&nbsp;

 Responsibilities Job Summary:

Under the direction of the Manager for administrative matters and the Medical Director assigned to the section for medical matters, plans, organizes and coordinates the work and employees of the section. Maintains accreditation standards, quality control and inventory.&nbsp; Selects, trains, evaluates, counsels and discharges employees.&nbsp; Maintains section in accordance with the goals and policies of the department and the institution.&nbsp; Maintains budgetary control.&nbsp; Works at bench when required.&nbsp; Serves as inspector for CAP.&nbsp; Participates in Laboratory Ward Rounds (customer service program).&nbsp; Coordinates student rotations.

Job Responsibilities:

<ul>
<li>Demonstrates up-to-date job knowledge. Demonstrates knowledge of, and adherence to, department policies and procedures.&nbsp;</li>
<li>Completes work assignments in a timely manner. Serves as a working coordinator of the section.&nbsp;</li>
<li>Assigns schedules and reviews the work of staff to insure that tests are performed in accordance with prescribed standards and the deadlines are observed.</li>
<li>Maintains an adequate number of qualified, competent staff following departmental and institutional policies and procedures.&nbsp;</li>
<li>Maintains knowledge of and compliance with regulatory and accreditation requirements. </li>
<li>Maintains required records in accordance with accreditation requirements.&nbsp;</li>
<li>Sets up and monitors appropriate internal and external quality control for instruments and test correcting problems as necessary.&nbsp;</li>
<li>Responsibility for inventory and ordering of supplies for the section. Makes recommendations for standing orders. </li>
<li>Compares cost and quality of supplies. </li>
<li>Prepares procedure manual, including biennial review in accordance with departmental formats and accreditation guidelines. </li>
<li>Maintains test section “Activity Menu” and notifies the Manager in advance whenever a test is to be added or deleted.&nbsp;</li>
<li> Is responsible for preventative maintenance in the section. Makes periodic replacements in accordance with prescribed procedures.</li>
<li>Adheres to safety (Universal Precautions), infection control and hazardous materials policies. </li>
<li>Maintains compliance in the section and notifies the Manager if there are problems that require work orders of equipment.&nbsp;</li>
</ul>
Job Requirements:

<ul>
<li>Bachelor’s degree (or foreign equivalent)&nbsp;in Clinical Laboratory, Medical Technology, Chemical, or Biological Science (or equivalent)&nbsp;and</li>
<li>3 years of Medical Technology experience.</li>
<li>MT or MLS (ASCP) Certificate.</li>
</ul>
 
PI2a427e28d556-25405-39078447

Laboratory Supervisor - Core Lab

<h3>Job Description</h3>
Job Title : Research Associate ( Research Assistant )
Location : South San Francisco - 94080
Duration : 12 Months 
Job Description : 
<ul>
<li>B.S. in Biology, Biochemistry, Molecular Biology, or a related discipline, with 1+ years of industry experience in pharmaceutical or biotechnology settings.</li>
<li>Hands-on experience performing quantitative assays (e.g. ELISA), for the characterization of proteins, nucleic acids, viruses or other biological products.</li>
<li>Strong hands-on experience with sterile technique and mammalian cell culture, including cell maintenance, expansion, characterization, and banking.</li>
<li>Working knowledge of core molecular biology techniques (DNA/RNA/protein isolation, cDNA synthesis, RT-PCR, qPCR, digital PCR).</li>
</ul>
Experience working with Adeno-Associated Virus (AAV) is a plus

Research Assistant

<h3>Job Description</h3>
Job DescriptionJob Title: Production ChemistJob Description
We are seeking a skilled Production Chemist to join our team and contribute to our chemical manufacturing processes. You will be responsible for handling raw materials, operating manufacturing equipment, and ensuring that all chemical operations are performed according to specific formulas to create new chemical compounds.
Responsibilities
<ul>
<li>Handle and manage all raw materials for chemical operations.</li>
<li>Operate chemical manufacturing equipment and follow specific chemical formulas.</li>
<li>Collaborate with engineers, production personnel, and the analytical team to ensure product specifications are met.</li>
<li>Work closely with chemical engineers and R&amp;D personnel to scale up processes.</li>
</ul>
Essential Skills
<ul>
<li>Bachelor's degree in Chemistry or related scientific field.</li>
<li>Experience in chemical processing and manufacturing.</li>
<li>Ability to work with R&amp;D personnel, scale-up and process teams, operations, and laboratory settings.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in chemical synthesis.</li>
<li>Strong laboratory skills.</li>
</ul>
Work Environment
The role involves working in a chemical manufacturing setting. Initial training occurs Monday through Friday on first shift hours (6 am to 2:30/3:30 pm). After training, the schedule shifts to a weekend day shift from 6:00 am to 6:00 pm on Friday, Saturday, and Sunday.
Job Type &amp; Location
This is a Contract to Hire position based out of Milwaukee, WI.
Pay and Benefits
The pay range for this position is $29.50 - $29.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Milwaukee,WI.
Application Deadline
This position is anticipated to close on Jan 21, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Production Chemist

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom AssemblerJob Description
Join a dedicated and high-performing team at our new Grand Rapids, MI site, where you will play a crucial role in the production and packaging of components for medical devices. Your work will be instrumental in our mission to alleviate pain, restore health, and extend life for millions of people worldwide. This role involves working in a cleanroom environment with personal protective equipment including eyewear, ear plugs, hair net, and protective gowning.
Responsibilities
<ul>
<li>Perform a variety of tasks ranging from repetitive to non-repetitive production assembly operations following Good Manufacturing Practices and Standard Operating Procedures.</li>
<li>Work from visual aids, method layouts, diagrams, schematics, process flow sheets, and written or verbal assembly instructions.</li>
<li>Set initial layouts and use a variety of tools to prepare products.</li>
<li>Conduct continuity checks on work in process and completed items.</li>
<li>Conduct quality inspections on processing line in accordance with quality specifications.</li>
<li>Operate packaging machines and handle boxing and labeling materials.</li>
</ul>
Essential Skills
<ul>
<li>General labor skills in a cleanroom environment</li>
<li>Ability to follow assembly and production procedures</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in a cleanroom manufacturing environment is a plus</li>
<li>Experience using measuring devices and hand tools</li>
</ul>
Why Work Here?
Be part of a nationwide company that is committed to improving healthcare and saving lives. Enjoy an air-conditioned, sit-down job that offers a supportive and innovative work culture.
Work Environment
This position involves working in a cleanroom with required personal protective equipment. The role is scheduled for the 2nd shift, Monday through Friday, from 2:30 PM to 10:30 PM.
Job Type &amp; Location
This is a Contract to Hire position based out of Grand Rapids, MI.
Pay and Benefits
The pay range for this position is $20.00 - $20.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Grand Rapids,MI.
Application Deadline
This position is anticipated to close on Jan 21, 2026.

About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Assembler

<h3>Job Description</h3>
Job Description
Job Description
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As an Associate Research Coordinator, one will assist the research coordinator (CRC/CCRC) in conducting clinical trials. The associate research coordinator is responsible for collecting, processing, storing and handling clinical specimens (as needed), scheduling study subjects for study visits, and collecting, recording, and filing clinical research data. Additionally, the associate research coordinator conducts study visits under the supervision of a study coordinator or senior coordinator.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (<a href="http://www.qps.com" target="_blank">www.qps.com</a>) for more information and to see all current openings.
The Job
<ul>
<li>Ensuring GCP is followed throughout the entire study conduct.</li>
<li>Ensuring subject confidentiality.</li>
<li>Ensuring the subject or subject’s legal representative is provided with a copy of the signed and dated informed consent form.</li>
<li>Possess a sound and in-depth understanding of each protocol that has been assigned</li>
<li>Source document creation per Protocol requirements (if applicable) or as needed</li>
<li>Ensuring compliance with applicable MRA SOP’s/MRA Clinical Research SOP’s, Good Clinical Practice guidelines and regulations</li>
<li>Timely communication of study issues to the study coordinator</li>
<li>Screening, Enrollment, and Ongoing Study Procedures
<ol>
<li>Establish good rapport with potential study subjects</li>
<li>Conduct telephone screening process</li>
<li>Conduct Informed Consent Process (must complete Consenting Process module and quiz prior to consenting)</li>
<li>Clinical data collection such as vital signs, ECG recording, subject height and weight, etc.</li>
<li>Medical records retrieval and review</li>
<li>Laboratory specimen collection, processing and shipment (as needed)</li>
<li>Transporting clinical specimens to the laboratory</li>
<li>Study visits scheduling </li>
</ol>
</li>
</ul>
Requirements
<ul>
<li>Combination of relevant education &amp; experience that provides sufficient knowledge &amp; skills to ensure incumbent’s success in this role, such as: </li>
<li>High School Diploma, and/or </li>
<li>Experience in a similar role </li>
<li>Prior experience as a medical assistant or in an ancillary or allied health specialty a plus</li>
</ul>
Why You Should Apply
<ul>
<li>Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.</li>
<li>Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.</li>
<li>Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&amp;D and Short and Long-term Disability Insurance</li>
</ul>

QPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Associate Research Coordinator

<h3>Job Description</h3>
About the Role
We are seeking a detail-oriented Research Programs Specialist to support research funding, investigator support, and research education initiatives within a mission-driven organization. This role plays a key operational and administrative function across grant programs, reporting, financial coordination, and event support.
The ideal candidate is highly organized, comfortable managing multiple deadlines, and enjoys supporting research and professional development initiatives behind the scenes.
 
Key Responsibilities
Grant Administration &amp; Program Support
<ul>
<li>Conduct compliance checks on grant applications prior to review</li>
<li>Maintain submission trackers and reporting databases</li>
<li>Assist with grant review preparation, including reviewer materials</li>
<li>Update application statuses within online grant management systems</li>
<li>Support grant processing, monitoring, and closeout activities</li>
</ul>
Reporting &amp; Program Evaluation
<ul>
<li>Track awardee reports and deliverables</li>
<li>Generate and organize reporting data for internal stakeholders</li>
<li>Follow up with award recipients regarding outstanding reports</li>
<li>Assist with grant outcomes analysis and summary reporting</li>
</ul>
Financial &amp; Administrative Support
<ul>
<li>Prepare payment and travel reimbursement requests, including documentation collection</li>
<li>Submit approved requests for processing</li>
<li>Maintain funded award tracking tools and checklists</li>
<li>Support financial stewardship across research-related programs</li>
</ul>
Meetings, Events &amp; Publications
<ul>
<li>Assist with planning and preparation for professional meetings and educational events</li>
<li>Provide logistical and material support for conferences and workshops</li>
<li>Draft outlines and assist with content preparation for research-related communications</li>
<li>Support internal publication and article development as needed</li>
</ul>
Operations &amp; Clerical Support
<ul>
<li>Maintain shared workspaces and inventory related to program operations</li>
<li>Prepare printed materials, binders, signage, and shipping materials for events</li>
<li>Support general office organization and administrative tasks</li>
</ul>
 
Qualifications
<ul>
<li>Bachelor’s degree preferred (health science, research, or related field a plus)</li>
<li>Experience in research, grants, or program administration strongly preferred</li>
<li>Willingness to attend evening calls (approximately 3–6 per month)</li>
<li>Availability for limited weekend work (3–5 times per year)</li>
</ul>

Research Programs Specialist

<h3>Job Description</h3>
Head of Research
San Mateo, CA | Full-Time
 
About Sankhara
Sankhara is a groundbreaking private equity fund dedicated to collecting, protecting and preserving the human experience through extraordinary physical assets. Rare books, maps, religious artifacts, classic cars, cultural landmarks, iconic sports memorabilia, and more - each with a unique story that shapes history. With a 100-year vision, our mission is to democratize ownership of history, making it accessible to the masses and protected by us, the philosopher-builders fostering a shared world.
 
The Role
Sankhara is hiring a Head of Research - a disciplined, highly capable, and deeply curious research leader who will be responsible for building, leading, and executing the research backbone of the firm.
 
This is not an academic role. This is not theoretical. This is a role for someone who has done serious institutional-grade research before - ideally on rare physical assets. Someone who understands how world-class analysis is constructed, how credibility is earned, and how research must stand up to auditors, LP diligence, skeptics, and historians alike. Someone who can think with commercial judgment and cultural reverence, while maintaining uncompromising standards of truth, rigor, provenance, and documentation.
 
You will work directly with the President and CEO. You will be deeply hands-on, producing research personally while building the frameworks, governance, agentic AI systems, and eventually a research function that scales. You will leverage your own expertise while building a trusted network of cultural, historical, technical, academic, and category experts - knowing when to utilize outside specialists.
 
If you want to help ensure that Sankhara not only acquires treasures, but understands them with depth, integrity, and authority - this is that opportunity.
 
What You Will Do
Asset-Level Research and Diligence
<ul>
<li>Lead research supporting potential acquisitions across all Sankhara verticals.</li>
<li>Develop, maintain, and continuously elevate the firm’s research methodology and standards.</li>
<li>Conduct primary and secondary research on provenance, authenticity, cultural importance, historical relevance, and risk considerations.</li>
<li>Produce structured, defensible research briefs to support investment decisions.</li>
<li>Where necessary, engage, manage, and coordinate subject matter experts, researchers, historians, scientists, and technical authorities.</li>
<li>Ensure research supports responsible decision-making, not storytelling bias.</li>
</ul>
 
Institutional Credibility and Governance
<ul>
<li>Design and maintain research frameworks that withstand institutional scrutiny.</li>
<li>Ensure research is audit-ready, organized, documented, and verifiable.</li>
<li>Support LP diligence needs through clear, high-quality research outputs.</li>
<li>Partner with legal, finance, and operations to ensure alignment between research, compliance, and governance expectations.</li>
<li>Contribute to clear standards around provenance management and authenticity validation.</li>
<li>Build trust and confidence with internal stakeholders by being the steady, disciplined truth source.</li>
</ul>
 
Thought Leadership and Scholarly Rigor
<ul>
<li>Help establish Sankhara as a serious, credible, intellectually grounded institution.</li>
<li>Produce high-quality materials as needed for Board review, executive decision-making, and strategic thinking.</li>
<li>Support the development of internal knowledge infrastructure across categories and themes.</li>
<li>Identify emerging cultural and thematic research areas relevant to future acquisitions.</li>
<li>Where appropriate, support external-facing thought leadership, while always anchoring in substance over hype.</li>
</ul>
 
Execution, Leadership, and Enablement
<ul>
<li>Build and lead the Research function over time.</li>
<li>Build out and maintain agentic AI systems for the Research function. </li>
<li>Be highly hands-on in the near term, personally doing a meaningful portion of research work.</li>
<li>Create documentation systems, workflow tools, and research architecture that scale.</li>
<li>Know when to leverage outside experts and when to execute directly.</li>
<li>Where useful, thoughtfully introduce process improvements, technology, tooling, or automation (including AI where appropriate) to enhance speed and rigor - without compromising standards.</li>
<li>Operate with urgency, but never at the expense of quality or integrity.</li>
</ul>
 
Who We’re Looking For
Required
<ul>
<li>3–5+ years of formal research experience in environments such as Gartner, Sotheby’s, Christie’s, Bonhams, leading consulting research organizations, major museums, or equivalent.</li>
<li>Proven track record producing serious, structured, and defensible research.</li>
<li>Experience working in environments that require accuracy, auditability, and institutional credibility.</li>
<li>Ability to synthesize complex cultural, historical, financial, and contextual information into structured research outputs.</li>
<li>Hands-on, execution-first mentality while capable of building toward a broader function.</li>
</ul>
 
Preferred
<ul>
<li>Experience across cultural assets, rare collectibles, historical objects, museums, or heritage fields.</li>
<li>Experience in research supporting investment, diligence, or risk frameworks.</li>
<li>Exposure to working with CEOs, Boards, or executive leadership.</li>
<li>Comfort operating in a fast-moving, ambitious environment without sacrificing rigor.</li>
</ul>
 
What Success Looks Like
<ul>
<li>Sankhara develops an institutional-grade research backbone that is highly respected internally and externally.</li>
<li>Research materially strengthens investment decisions and institutional confidence.</li>
<li>LPs, auditors, advisors, and partners trust Sankhara’s depth, seriousness, and documentation.</li>
<li>The firm’s narrative becomes stronger because its foundation is unassailably true.</li>
<li>The executive team sleeps better knowing research is disciplined, responsible, and world-class.</li>
</ul>
 
Compensation
Competitive base compensation, performance-based bonus opportunity, and long-term upside participation potential (including equity, carry, and/or token-linked economics depending on structure).
 
Why This Role Matters
Sankhara is building something designed to last centuries. This role ensures that what we collect, protect, and share with the world is deeply understood, properly honored, defensible, and documented - preserving not only treasures themselves, but the truth and meaning behind them.
 
If that excites you - we’d love to meet you.
 
How to Apply
Interested candidates should apply through LinkedIn and/or submit their resume and a cover letter detailing their qualifications and experience to <a href="mailto:blake@sankhara.com" target="_blank">blake@sankhara.com</a>.
 
Join us at Sankhara and help us on this incredible journey!

Head of Research

<h3>Job Description</h3>
Job Description
Mission Driven, Community Focused About | Charles R. Drew University of Medicine and Science (cdrewu.edu)
Charles R. Drew University is located in the Watts-Willowbrook area of South Los Angeles and was founded in 1966 in the wake of the Watts uprising. CDU was founded to address inadequate medical care in the region and to provide equitable medical education opportunities for underrepresented students. CDU is strongly invested in the local and regional community. The university leads multiple partnerships and programs to provide equitable healthcare resources in a variety of South Los Angeles neighborhoods.
Under the direct supervision of the Project PI/s the Research Associate is responsible for a broad range of routine to moderately complex research duties, including working with mice, perform techniques such as MTT assay, immunohistochemistry, RNA extractions, real time PCR, western blots and biochemical determinations. The long-term goal of our studies is to investigate signaling pathways involved in therapeutic response as well as drug resistance in cancer, and to identify novel agents in cancer chemoprevention and treatment. To achieve these goals, we use multidisciplinary experimental approaches applying both in vitro and in vivo animal models, and high-throughput screening approaches through collaboration with experts in the field.
Essential Duties and Responsibilities:
<ul>
<li>Duties assigned to this title will require an in-depth knowledge of a specialized field, process, or discipline and may involve organizing and implementing complex research plans, the development of methods of research, testing and data collection, analysis and evaluation, and writing reports (weekly reports and progress reports) containing descriptive, analytical and evaluative content.</li>
<li>The duties will require the exercise of independent discretion and judgment in carrying out research activities within the predetermined research scope and methodology.</li>
<li>Participates in research studies to include molecular biology, immunohistochemistry, flow cytometry, MTT assay, RNA extractions, real time PCR, western blots, biochemical determinations, cell transfections, anesthesia, injections, aseptic work, animal handling, and tissue excision.</li>
<li>Maintains inventory and supplies needed for the research lab.</li>
<li>Coordinates from various collaborating departments and collaborates with</li>
<li>Responsible for statistical analyses of data and writing up</li>
<li>Demonstrates leadership in presentation materials and manuscript</li>
<li>Assists divisional staff members and other collaborators in the</li>
<li>Analyzes and records research data, submit weekly reports to the</li>
<li>Maintains related correspondence and regulatory paperwork.</li>
<li>Presents research papers at</li>
<li>Assist the program in mentoring and providing oversight for student</li>
</ul>
Other Duties and Responsibilities:
<ul>
<li>Perform other related duties as</li>
</ul>
Qualifications/Requirements:
 EDUCATION:
<ul>
<li>Regionally accredited doctoral degree (Ph.D., ) or master’s degree required in biomedical science related area.</li>
</ul>
EXPERIENCE:
<ul>
<li>Three years related experience in molecular biology, immunohistochemistry, RNA extractions, real time PCR, western blots, biochemical determinations, plasmid preparation and analysis, cell transfections; anesthesia, injections, aseptic work, animal handling, and tissue excision.</li>
<li>Prior statistical experience with quantitative data analysis and proficiency with commonly used statistical/numerical</li>
<li>Animal self-administration experience is a</li>
</ul>
KNOWLEDGE/ABILITY/SKILLS:
<ul>
<li>Laboratory skills needed including ability to perform biochemical assays and molecular biology</li>
<li>Computer</li>
<li>Written and oral communication</li>
<li>Able to troubleshoot and resolve technical</li>
<li>Committed to a career in biomedical</li>
</ul>
COMPLEXITY:
<ul>
<li>The ability to perform highly detailed work with sustained attention and care while providing/obtaining information on numerous inquiries is paramount to success in this position.</li>
</ul>
PHYSICAL DEMANDS:
<ul>
<li>The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Occasional stooping. Frequent standing. Constant walking, sitting, climbing, reaching high/low levels, finger movement, feeling, speaking clearly, hearing conversationally, and seeing far and near.</li>
</ul>
WORK ENVIRONMENT:
<ul>
<li>The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</li>
</ul>
MENTAL DEMANDS:
<ul>
<li>The mental demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Frequent work on a variety of unrelated tasks. Constant calculating interrupted work, work on a variety of interrelated tasks, and use of sustained concentration, reasoning, judgment, resourcefulness, analytical ability, and ingenuity.</li>
</ul>
SPECIAL REQUIREMENTS:
<ul>
<li>Ability to work effectively with a diverse</li>
<li>The ideal candidate will be seeking a career in Biomedical Science and able to make a long-term commitment.</li>
</ul>
Compensation:
<ul>
<li>$70,304.00</li>
</ul>
Position Status: 
<ul>
<li>Exempt, Full-time </li>
</ul>
Work Location: 
<ul>
<li>On-site</li>
</ul>
Conditional Employment:
The employment status of this position is classified as “Conditional.” Conditional employment means that the job exists contingent upon continued funding and limitations of restricted funds or, the duration of a specific program, project, grant, or contract. Since your salary is funded by: Signaling Mediators, G0075520, End Date: April, 30, 2026, and ACS Pilot Project, End Date: April 30, 2026, your position is contingent upon the continued receipt of these funds. Continuation of your position is dependent, in part, upon funding availability. Furthermore, no work may be performed after the grant end date(s) unless you have received an extension in writing from a Dean, Division VP, or Human Resources.
EEO Statement: Charles R. Drew University is committed to Equal Employment Opportunity. Applicants will be considered without regard to gender, race, age, color, religion, national origin, sexual orientation, genetic information, marital status, disability or covered veteran status.
Fair Chance Statement: Charles R. Drew University of Medicine and Science will consider qualified applicants, including those with criminal histories, in a manner consistent with state and local “Fair Chance” laws.

Research Associate

<h3>Job Description</h3>
Job Description
M-F, 8 am to 5 pm 
 
Summary
The Research Coordinator will support and oversee the execution of multiple clinical research studies across inpatient and outpatient units at The Menninger Clinic. This position may contribute to clinic-wide outcomes research as well as focused research projects examining topics such as mental health, predictors of treatment response, resilience, recovery and relapse, and emerging and innovative interventions.
The role involves direct interaction with patients and clinical staff, coordination with academic and institutional partners, and administrative responsibilities related to regulatory compliance, data quality, and reporting. Depending on the study, the Research Coordinator may also accompany participants to off-site locations (e.g., academic medical centers) for study procedures such as neuroimaging.
This position offers a unique opportunity for meaningful patient-facing research experience within a nationally recognized psychiatric hospital and is particularly well-suited for individuals seeking advanced training in medicine, psychology, social work, public health, or related fields.
Key Functions
Study Coordination &amp; Operations
<ul>
<li>Oversee day-to-day execution of multiple research protocols across Menninger Clinic units (inpatient and/or outpatient).</li>
<li>Serve as a primary point of contact between research teams and Principal Investigator(s).</li>
<li>Track study progress and communicate recruitment, retention, and milestone updates to investigators.</li>
<li>Coordinate research workflows and, when applicable, supervise research assistants or trainees.</li>
<li>Prepare and maintain study-related documentation, including protocols, manuals of procedures, consent forms, and correspondence.</li>
</ul>
Regulatory &amp; Compliance
<ul>
<li>Prepare, submit, and manage Institutional Review Board (IRB) applications, amendments, continuing reviews, and related correspondence.</li>
<li>Ensure adherence to institutional policies and federal and sponsor regulations.</li>
<li>Maintain accurate and up-to-date regulatory binders and study records.</li>
</ul>
Participant Interaction &amp; Clinical Research Activities
<ul>
<li>Recruit, screen, consent, and enroll patients across inpatient and outpatient programs into research studies.</li>
<li>Communicate with participants via face-to-face interactions, phone calls, and email throughout their participation.</li>
<li>Conduct standardized assessments and clinically complex research or diagnostic interviews, as appropriate to training and protocol requirements.</li>
<li>Schedule and coordinate research-related appointments, tests, and procedures (e.g., laboratory tests, imaging, behavioral tasks).</li>
<li>Coordinate and attend off-site study visits when required (e.g., MRI scans at Baylor College of Medicine or other partner institutions).</li>
<li>Communicate relevant study participation information to clinical teams to support coordinated and safe patient care.</li>
</ul>
Data Management &amp; Outcomes Research
<ul>
<li>Ensure timely and accurate data collection across studies.</li>
<li>Perform data cleaning and quality assurance checks, to ensure data are analysis-ready.</li>
<li>Generate and distribute research and outcomes reports for participants, clinicians, investigators, and other stakeholders in a timely manner as appropriate given the study.</li>
<li>Support longitudinal follow-up and retention efforts for outcomes research.</li>
</ul>
Research Dissemination &amp; Professional Development
<ul>
<li>Work closely with clinician-scientists and interdisciplinary research teams and receive mentorship in clinical research methods and scientific communication.</li>
<li>Participate, as appropriate and based on interest and performance, in data analysis, abstract preparation, conference presentations, and manuscript development.</li>
<li>Participate, as appropriate and based on interest and performance, in research meetings and contribute to discussions related to study design, interpretation, and dissemination.</li>
</ul>
Administrative &amp; Resource Management
<ul>
<li>Coordinate acquisition and management of research supplies and equipment.</li>
<li>Assist with budget tracking and financial oversight for research projects.</li>
<li>Perform other research-related duties as assigned.</li>
</ul>
Education
Required: Bachelor’ degree.
Preferred: Bachelor’s degree in psychiatry, psychology, social work, neuroscience, public health, or other degrees translational mental health research.This position is ideal for highly motivated early-career professionals seeking hands-on clinical research experience prior to applying to medical school, graduate programs (PhD, PsyD, MPH), or other health-related training programs. 

Why Join The Menninger Clinic Research Team?
The Menninger Clinic is a nationally recognized leader in psychiatric care and research. This role offers exceptional exposure to complex mental health populations, innovative research initiatives, and close collaboration with experienced clinician-scientists. The Research Coordinator position provides a strong foundation for future careers in medicine, psychology, neuroscience, public health, and clinical research.

Research Coordinator, Outpatient

<h3>Job Description</h3>
Job DescriptionWanted: Geotechnical Engineer - Senior, Project, and Associate Levels Don't Miss Out On This GREAT Opportunity. Apply today! This Jobot Job is hosted by: Stephen Niedringhaus Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $100,000 - $170,000 per year 
A bit about us:
 ** HIRING - Experience Geotechnical Engineer - Senior, Project, and Associate Levels Don't Miss Out On This GREAT Opportunity. Apply today! ** Award-winning Geotechnical and Civil Engineering Firm continues to grow. We have a lot of work that needs to be done and done right! If you want to join a "Family-Like" company, do not wait, apply today. For almost 60 years, we have built our reputation as a trusted consultant for some of the most challenging and recognizable construction, and Civil &amp; Geotechnical Engineering projects across Southern California because we do things a little differently! Our projects range from private developers and residential projects to high-profile public works infrastructure projects. Don't miss out on this excellent career opportunity. Interviews are going on now. 
Why join us?
 Geotechnical Engineers - Senior, Project, and Associate Levels 
<ul>
<li> Competitive Base Salary - $100,000 to $170,000 depending on experience and qualifications</li>
<li> Flexible Work Schedules - Work | Life Balance!!!</li>
<li> "Family-Like" Work Atmosphere!!!</li>
<li> Accelerated Career Growth!!!</li>
<li> Medical, Dental, Vision, Life Insurance, HSA contributions, and matching 401(k)</li>
<li> Profit Sharing Bonus</li>
<li> Paid Holidays</li>
</ul>
 And so much more!!! 
Job Details
 You will join our growing team of Engineers and Geologists. Key Responsibilities and Duties 
<ul>
<li> Join a dynamic team of engineers and geologists</li>
<li> Oversee and design geotechnical field investigations (drilling, sampling, lab testing)</li>
<li> Analyze subsurface and geologic data for modeling and design</li>
<li> Perform geotechnical analyses for slope stability, liquefaction, foundation capacity, etc.</li>
<li> Prepare detailed geotechnical reports and design recommendations</li>
<li> Manage projects from proposal to delivery and client coordination</li>
<li> Use specialized software for analysis, mapping, and design</li>
<li> Collaborate with interdisciplinary teams across civil, structural, and pavement engineering</li>
</ul>
 Must-Have and Preferred Skills: 
<ul>
<li> Must have: California Professional Engineer (PE) license and B.S. in Civil Engineering</li>
<li> 8+ years of geotechnical engineering experience</li>
<li> Strong expertise in geotechnical investigations, analysis, and design</li>
<li> Proficiency with software such as LPILE, Slope/w, FLAC, CPet-IT, SHAFT, PYWALL</li>
<li> Experience preparing technical geotechnical reports</li>
<li> Project management experience including budgeting, proposals, and scheduling</li>
<li> Familiarity with AutoCAD and ESRI ArcGIS</li>
<li> GE license or Master’s in Geotechnical Engineering (preferred)</li>
</ul>
 Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policyCompany DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

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