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<h3>Job Description</h3>
Job DescriptionSalary: 
Launch Your Career in Public Affairs Competitive Intelligence
 
Program Start Date: March 2026
 
Launch your career at the intersection of politics, business, and strategy.
 
Delve Research is Washingtons premier strategic intelligence and risk advisory firm, equipping the advocates and practitioners of free enterprise with the insights they need to navigate high-stakes policy and reputational issues. Our clientsFortune 500 companies, trade associations, and advocacy coalitionsturn to us to make sense of complex and heavily scrutinized issues so they can protect their ability to innovate, invest, and grow.
 
Featured by The Washington Post, Politico, and other leading outlets, we combine a deep understanding of the stakeholders, dynamics, and reputational factors shaping public affairs with cutting-edge research techniques and AI-driven tools to deliver in-depth, actionable intelligence that drives results.
 
Why Join Us?
 
Our three-month, full-time, stipended Associate Training Program is the launchpad for recent graduates and early-career professionals who want to build a career in public affairs research and competitive intelligence.
 
Associates dont just observe from the sidelinesyoull work alongside our analysts to:
<ul>
<li>Analyze the people, organizations, and dynamics influencing high-stakes issues -- who can the client engage and work with? Whose efforts will they have to overcome?</li>
<li>Learn how to map stakeholder networks, track reputational threats, and understand who is shaping outcomes.</li>
<li>Turn open-source information into concise, actionable insights for senior executives and their public affairs teams.</li>
<li>Gain hands-on exposure to client work across industries such as energy, life sciences, financial services, AI and other technology sectors, as well as trade and other complex, sensitive policy and political issues.</li>
</ul>
 
Successful Associates will have the opportunity to advance into full-time Analyst roles upon completing the program.
 
Who Thrives Here?
 
Our most successful Associates share these qualities:
<ul>
<li>Commitment to advancing free enterprise and working with discretion You believe in the power of free markets and can be trusted with highly sensitive client strategies.</li>
<li>Exceptional research and writing skills You can take large volumes of information and craft clear, concise, actionable analysis under tight deadlines.</li>
<li>Curiosity and fast learning You quickly master unfamiliar industries, issues, and stakeholder networks.</li>
<li>Client-service orientation Youre motivated to help practitioners and advocates succeed, not to push your own agenda.</li>
<li>Proven initiative and leadership Experience running student organizations, political campaigns, or legislative projects under deadline pressure.</li>
<li>Relevant exposure Hands-on experience with a political campaign, association, lobbying or public affairs firm, or a Congressional or state legislative office is expected.</li>
</ul>
 
What Youll Do
 
As a Spring 2026 Research Associate, you will:
<ul>
<li>Complete intensive training in competitive intelligence research and analysis techniques.</li>
<li>Support analysts by producing stakeholder profiles, monitoring key actors, and contributing to issue-focused reports.</li>
<li>Track and synthesize information from news, social media, government filings, and other open sources.</li>
<li>Contribute to client deliverables and internal knowledge-building on sectors and issues central to our work.</li>
</ul>
 
Program Details
<ul>
<li>Program Dates: March 2026 May 2026 (full-time)</li>
<li>Location: Hybrid (Washington, D.C. office + remote flexibility)</li>
<li>Compensation: Stipend provided for the duration of the program</li>
</ul>
 
Ready to Launch Your Career?
Spots for the Spring 2026 class are highly competitive. Apply now to gain the skills, experience, and connections to build a career in public affairs consulting, strategic research, or competitive intelligence.

Research Associate - Spring 2026

<h3>Job Description</h3>
Job DescriptionSalary: $18.96 
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Fisheries Observer!!

A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is recruitingReef Fish and ShrimpFisheries Observersto work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Southeast Fisheries Science Center (SEFCS) aboard commercial fishing vessels.

The primary goals of the governments shrimp and reef fish observer programs are to provide quantitative biological, vessel, and gear-selectivity information for the southeastern shrimp fishery and Gulf of Mexico reef fish fishery. Observers deploy on commercial shrimp and reef fish vessels operating in the Gulf of Mexico and South Atlantic.If you ever wanted to make a difference, this is how.

Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between the fishing industry and fisheries scientists like yourself. In order to facilitate cooperation, fisheries observers collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen.Commit to the journey!

Click toLearn More about Becoming a Fisheries Observer

Observers record detailed information on the gear and fishing activity of the vessels. Observers work on deck on vessels ranging from 30 to 90 on trips roughly ranging from 1 to 45 days collecting data on fish catch and bycatch, and incidental takes such as marine mammals, seabirds and marine turtles. After attending a 3-week paid training in-person training in Galveston, TX observers are deployed from ports throughout the Gulf of Mexico and southern Atlantic states. Gear types assessed include but are not limited to shrimp trawl, bottom longline, modified buoy gear, bandit reel, and handline. Training projected for end of March/ April timeframe.

Accommodations and meal reimbursement during in person session of training are provided.Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.

This is a challenging job, and candidates must be mentally prepared to be away from home without access to internet or cellular telephone signal for multiple days and often weeks at a time. Candidates must be physically able to handle heavy lifting, working odd hours, and spending long days in rough seas. Many crews speak limited English compounding the effects of loneliness and isolation on long trips. Observing provides an excellent career in marine biology, as observers are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.

Compensation:Observersstarting pay is $19.33/hour. Dependent on enrollment in our H&amp;W benefit, observers may also be eligible for anadditional $4.57/hourfor the first 40 hours worked on each calendar week for a total of$23.90 hour. This is a fulltime position with benefits.Annually, observers earn between $35K - $55K a year dependent on their availability to deploy offshore and their personal sea day accomplishments. Observers will be paid a minimum of 8 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.

AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.

Travel is reimbursedin accordance with federal travel guidelines at an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.

Minimum Qualifications:
<ul>
<li>A bachelor's degree from an accredited college or university with a major in one of the natural sciences and a minimum of 30 semester hours or equivalent in the biological sciences</li>
<li>At least one undergraduate course in math or statistics.</li>
<li>All relevant course work must have been performed at a level acceptable for credit at the candidates academic institution.</li>
<li>Experience with data entry on computers.</li>
<li>Observer candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physicians certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
</ul>

Preferred Qualifications:
<ul>
<li>At-sea experience</li>
<li>The ability to work independently and live in close quarters with little to no communication for purposes other than safety status check-ins for up to 8 weeks. (phone, internet, email and other amenities are unavailable at-sea)</li>
<li>Coursework with dichotomous keys</li>
</ul>

Homeport:
Applicants must be currently living, or be willing to live within 50 miles of the Bayou La Batre, AL

Contact:
If you would like to apply for one of these exciting new openings, please click the following linkCareers Pageto submit the following information.

<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>3 to 5 academic/professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts.</li>
</ul>

All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to theTalent Teamor 774-770-5833

An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
 
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

Reef Fish and Shrimp Fisheries Observer - Bayou La Batre, AL

<h3>Job Description</h3>
Job Description
Our client is seeking a Geotechnical Engineer to support a wide range of site investigation, design, and construction support efforts. This role offers exposure to diverse project types and responsibilities, making it ideal for an engineer who wants hands-on experience, technical variety, and long-term career stability within a close-knit team.
Responsibilities
<ul>
<li>
Perform geotechnical investigations including soil borings, field observations, and laboratory review
</li>
<li>
Prepare geotechnical reports, recommendations, and construction support documentation
</li>
<li>
Support construction materials testing activities and review test results for compliance
</li>
<li>
Coordinate with project stakeholders including contractors, inspectors, and internal team members
</li>
<li>
Assist with project planning, scheduling, and technical problem-solving across multiple project types
</li>
</ul>
Requirements
<ul>
<li>
Bachelor's degree in Civil or Geotechnical Engineering
</li>
<li>
EIT required; Professional Engineer (PE) license preferred
</li>
<li>
Construction materials testing experience required
</li>
<li>
Proficiency with AutoCAD, GEO5, and Microsoft Office (Word, Excel, PowerPoint)
</li>
<li>
Strong technical writing, organizational, and communication skills
</li>
<li>
PMP certification is a plus but not required.
</li>
</ul>
Why Join Our Client This opportunity offers the chance to join a well-established engineering firm with deep roots in its market and a reputation built over decades. You'll work in a small, collaborative environment with long-tenured professionals, gain exposure to a broad range of geotechnical work, and be part of a company that values stability today while planning for thoughtful growth in the future.
About J.Riley Recruitment J.Riley Recruitment is THE Veteran-Owned Business connecting Military Veterans and Top Professionals with the Best Companies. Since our founding in 2020, J.Riley Recruitment has leveraged over a decade of Talent Acquisition expertise to deliver exceptional results. Our network extends coast to coast, empowering organizations nationwide to overcome challenges and achieve success.
Built on a foundation of integrity, discipline, and precision, we bring operational excellence and adaptability to recruitment that defines top-tier organizations. By understanding our clients' unique challenges and aligning with their goals, we deliver high-performing talent that drives mission-focused outcomes.

Geotechnical Engineer

<h3>Job Description</h3>
Job Description
Role: Sr. Analytical Chemist
Location: Salisbury, NC
Pay Rate Range: $140,000 - $190,000 / yr. DOE
Location: Salisbury, NC (Fully Onsite – 5 Days/Week)
Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Relocation Assistance: Available
Employment Type: Full-Time, Permanent
Benefits: Comprehensive benefits package available
 
Are you looking for a growth opportunity for a reputable company with a positive work environment? 

Our client is looking for a Sr. Analytical Chemist to join their team. Please contact us today to discuss this opportunity!
 
About the Role
We are seeking a Senior Analytical Chemist to join our specialty chemicals organization focused on personal care applications (e.g., shampoos, body washes, and surfactant-based formulations). This is a highly technical, hands-on role supporting product development, troubleshooting, and analytical excellence within a collaborative laboratory environment.

The position is fully onsite in Salisbury, North Carolina, which is commutable from the Greater Charlotte area and located between Charlotte and Greensboro. Occasional travel to nearby facilities and international collaboration opportunities may be available.
 
Key Responsibilities
· Design and execute advanced analytical and wet chemistry methods to support personal care and surfactant-based products
· Perform and interpret analyses using chromatography (GC, HPLC) and complementary analytical techniques
· Apply expertise across spectroscopy, thermal analysis, mass spectrometry, microscopy, and physical testing
· Conduct wet analytical techniques including titrations, solids analysis, salts, and activity testing
· Partner with R&amp;D, manufacturing, and quality teams to solve complex formulation and performance challenges
· Document methods, results, and technical findings clearly and thoroughly
· Contribute to continuous improvement, method development, and best laboratory practices
· Serve as a technical resource and mentor within the analytical chemistry team
 
Required Qualifications
· PhD in Analytical Chemistry, Organic Chemistry, or a closely related discipline
· Strong hands-on experience with chromatography (GC, HPLC) and wet chemistry
· Demonstrated expertise in surfactant chemistry and personal care or specialty chemicals
· Background in analytical techniques including spectroscopy, thermal, physical, mass spectrometry, and microscopy
· Passion for laboratory-based problem solving and applied chemistry
 
Preferred Qualifications
· 5–10 years of industry experience in specialty chemicals or personal care
o Exceptional recent PhD graduates with strong hands-on experience will be considered
· Experience working with consumer or personal care formulations (shampoos, body washes, cleansers)
· Stable career progression with demonstrated long-term commitment in prior roles
· Educational background from a well-recognized technical institution is a plus
Note: This role is not aligned with polymer chemistry-focused backgrounds.
 
Compensation &amp; Benefits
· Best in industry compensation and comprehensive benefits package
· Relocation assistance provided
· Long-term growth and career stability within a technically driven organization
 
Work Environment
· Fully onsite laboratory role (no remote or hybrid option)
· Collaborative, high-accountability culture focused on technical excellence
· Opportunity for domestic and potential international collaboration
 
Why choose Addison?
• Pay: We negotiate high salaries using U.S. Bureau of Labor Statistics
• Benefits &amp; Bonuses: You are eligible for medical, dental, vision insurance benefits, 401K, and monetary bonuses
• Permanent Employment: Many of Addison’s job openings lead to potential permanent employment
• Connections: You connect directly with hiring managers from renowned organizations
• Options: You are presented multiple employment options near your home
• Professional Development: You are provided hiring process advice, resume revision, and employment term negotiation

Addison Group is an Equal Opportunity Employer. Addison Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Addison Group complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. Reasonable accommodation is available for qualified individuals with disabilities, upon request.
 
IND 005-009

Sr. Analytical Chemist

<h3>Job Description</h3>
Job Description
Location: Swiftwater, PA
**This role will require full-time presence at our client site in Swiftwater, PA**
**This role is NOT eligible for relocation assistance**

The Zifo Lab Computing Analyst provides technical laboratory services, including multivendor instrument, information technology and validation/compliance services when applicable. The individual will provide the consulting skills required to analyze customer needs and gaps to propose solutions for the desired state. He or she will work with business users and managers of customers in conjunction with the internal Zifo support team. 
Requirements
Responsibilities:
<ul>
<li>Provide technical support of customer laboratory environments, typically for computers that are integrated with instrumentation</li>
<li>Manage lab computing aspects of installing new, retirement and relocation of equipment</li>
<li>Implement Windows based security</li>
<li>Ensure adherence to client’s corporate policies through periodic reporting and compliance programs</li>
<li>Act as the technical support contact for field service engineers and external vendors</li>
<li>Provide technical subject matter expertise for new system validation and change management efforts</li>
<li>Document procedures, policies, troubleshooting and best practices</li>
<li>Create and maintain a physical inventory of lab equipment, PC’s, software, and any other information pertinent to the environment if applicable</li>
<li>Perform system preventative maintenances based on client’s schedule, if applicable</li>
</ul>
Required Skills:
<ul>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests</li>
<li>Ability to troubleshoot complex instrument and technology issues</li>
<li>Strong oral and written communication skills</li>
<li>Ability to identify, track and complete tasks for multiple projects</li>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code</li>
</ul>
Qualifications:
<ul>
<li>Bachelor of Science in computer science, life science or equivalent industry experience</li>
<li>3+ years of relevant technical experience including (but not limited to); Windows technologies, networking, remote computing and backup systems</li>
<li>Excellent customer service skills complemented by an ability to listen to and interpret client requests</li>
<li>Ability to troubleshoot complex instrument and technology issues</li>
<li>Strong oral and written communication skills</li>
<li>Ability to identify, track and complete tasks for multiple projects</li>
<li>Knowledge of laboratory safety practices as defined by the company and/or customer’s site safety code</li>
<li>Experience with virtual machine support (preferred)</li>
<li>Experience with scientific instrumentation (preferred) </li>
</ul>

Benefits
About Zifo:
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team’s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 7 of the Top 10 Biopharma companies.
We look for Science – Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a “no doors” policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda – technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

GxP Lab Computing Analyst

<h3>Job Description</h3>
Job Description
Job post summary
Date posted:&nbsp;January 12, 2026
Pay:&nbsp;$30.00 - $40.00 per hour
Job description:
R&amp;D Chemist
Job Category:&nbsp;Professional Background Check:&nbsp;7-year standard Employment Type:&nbsp;Full-time Pay:&nbsp;30-35 but will pay up to 40 on the right candidate Shift:&nbsp;Monday-Friday 7am to 330pm
Position Overview
We are seeking an experienced R&amp;D Chemist to support the development, improvement, and scale-up of adhesive products. This role plays a hands-on part in formulation, testing, and technical support across multiple product lines. The ideal candidate is detail-oriented, collaborative, and comfortable moving between lab work, documentation, and cross-functional problem-solving.
The scope of work includes solvent-based and water-based adhesives, hot melts, and rubber-based technologies applied through brush and spray methods across a variety of substrates.
Key Responsibilities
Formulation &amp; Development
<ul>
<li>Design, formulate, and document adhesive products from concept through scale-up</li>
<li>Lead development efforts for assigned product lines</li>
<li>Support batch scale-up and transition from lab to manufacturing</li>
</ul>
Product Support &amp; Optimization
<ul>
<li>Maintain and update existing formulations as needed</li>
<li>Address customer questions, technical issues, and product complaints</li>
<li>Support product certifications and documentation requirements</li>
</ul>
Testing &amp; Quality Collaboration
<ul>
<li>Apply appropriate performance testing, QC procedures, and application methods</li>
<li>Partner with Quality Control teams to ensure product consistency and compliance</li>
</ul>
Cross-Functional Collaboration
<ul>
<li>Work closely with project management to drive organized and efficient product development</li>
<li>Provide technical support to manufacturing when required</li>
<li>Present technical findings to internal business teams and collaborate with external suppliers</li>
</ul>
Required Qualifications
<ul>
<li>Bachelor’s degree in Chemistry, Biology, Engineering, or a related field preferred</li>
<li>Minimum of 3 years of hands-on experience with:</li>
<li>Adhesion and rubber-based chemistry</li>
<li>Solvent-based chemical systems</li>
<li>Adhesive formulation and development</li>
<li>Strong understanding of laboratory documentation and development processes</li>
<li>Ability to communicate technical information clearly to non-technical stakeholders</li>
</ul>
Skills &amp; Attributes
<ul>
<li>Self-motivated and well-organized</li>
<li>Strong collaboration and teamwork skills</li>
<li>Comfortable taking ownership of technical decisions</li>
<li>Able to manage multiple projects and priorities effectively</li>
</ul>
Job Types: Full-time, Temp-to-hire
Benefits:
 
<ul>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Vision insurance</li>
</ul>
 
Work Location: In person
Company DescriptionLiberty Staffing USA is a diverse culture-minded staffing company run by skillful staffing professionals with decades of combined experience. Our ultimate goal is to place the right people in the right jobs, provide our customers with premium service. 
<h3>Company Description</h3>
Liberty Staffing USA is a diverse culture-minded staffing company run by skillful staffing professionals with decades of combined experience. Our ultimate goal is to place the right people in the right jobs, provide our customers with premium service.

R&D Chemist

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Statistical Genetics &amp; Human Biobanks Intern will support Translational Genetics research at Arrowhead Pharmaceuticals by developing AI-augmented workflows that integrate large-scale global human biobank data to identify disease-relevant genes for RNAi target discovery. This internship offers hands-on experience applying statistical genetics, functional genomics, and causal inference methods to real-world therapeutic discovery challenges. The intern will collaborate closely with computational and translational scientists to generate high-confidence, genetically supported hypotheses that inform target prioritization and decision-making.
This is an 11-week Summer Internship Program paying $27.00 per hour and this role requires full-time, onsite work five days per week at the designated location.
Responsibilities
<ul>
<li>Support analysis of large-scale genetic and biomedical datasets to help identify disease-relevant signals.</li>
<li>Assist in developing and applying analytical and AI-enabled workflows for data integration, interpretation, and reporting.</li>
<li>Contribute to evidence synthesis and data summarization to support research and target evaluation efforts.</li>
<li>Help assess consistency and robustness of findings across multiple datasets or sources.</li>
<li>Prepare clear summaries, visualizations, or reports to communicate results to the project team.</li>
<li>Present updates and findings during team meetings and participate in scientific discussions.</li>
<li>Collaborate with scientists and computational team members on research projects and special initiatives.</li>
</ul>
Requirements
<ul>
<li>Currently pursuing a PhD in Statistical Genetics, Human Genetics, Computational Biology, Bioinformatics, Biostatistics, or a closely related field.</li>
<li>Hands-on experience analyzing data from at least one major human biobank.</li>
<li>Proficiency in Python and/or R for statistical genetics and data analysis workflows.</li>
<li>Familiarity with GWAS summary statistics, rare variant interpretation (pLoF/GoF), and functional genomics datasets such as eQTL and pQTL.</li>
<li>Strong understanding of population genetics, genetic architecture, and variant-to-gene mapping.</li>
<li>Ability to translate genetic association evidence into actionable therapeutic hypotheses.</li>
<li>Excellent verbal and written communication skills and ability to collaborate in a cross-functional research environment.</li>
</ul>
Preferred 
<ul>
<li>Proficiency with statistical genetics and functional genomics tools such as REGENIE, SAIGE, TWAS frameworks, Mendelian randomization packages, and colocalization methods.</li>
<li>Demonstrated ability to interpret pLoF/GoF variants and integrate eQTL/pQTL data with GWAS findings to identify causal genes and pathways.</li>
<li>Experience developing AI- or LLM-assisted analytics for evidence synthesis, automation, or variant-to-gene mapping.</li>
<li>Strong interest in translational genetics, RNAi therapeutics, and data-driven target discovery.</li>
</ul>
California pay range $11,440—$11,440 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Summer Intern, Statistical Genetics & Human Biobanks

<h3>Job Description</h3>
Job Description
The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.
START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.
We are hiring an Administrative Research Assistant at our START Mountain office located in West Valley City, UT. This is an on-site role with day shift working hours. This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation.
Schedule: Monday through Friday, 8am - 4pm
Essential Responsibilities:
<ul>
<li>Collect, de-identify, enter, and transmit clinical data in CRFs, including images, lab results, and ECGs; resolve corrections and queries for investigational drug studies.</li>
<li>Collaborate with Clinical Research Coordinators to ensure data accuracy, query resolution, and protocol adherence.</li>
<li>Assist with study setup, including Eligibility, Study Schedules, Flow Sheets, and CTMS upkeep (e.g., tracking visits, IRB re-consents, SAEs, and deviations).</li>
<li>Maintain current data transmissions, provide support to onsite/remote monitors, and ensure compliance with regulations and EDC system guidelines.</li>
<li>Contact patients for follow-up per protocol and attend study-related meetings (e.g., site initiation, Roster, and Forms Committee).</li>
<li>Support lab certification by identifying lab facilities and normal lab values for assigned studies.</li>
<li>Communicate with accounts receivable staff as needed and perform other tasks as assigned.</li>
</ul>
Required Education and Experience:
<ul>
<li>High School diploma or equivalent.</li>
<li>One year of research administrative experience within a healthcare, pharmaceutical, or research organization.</li>
<li>Knowledge and training in general office administration skills, including computer applications, filing systems, etc.</li>
<li>Familiarity with medical terminology.</li>
<li>Strong organizational skills and a sense of timeliness in completing projects.</li>
<li>Must be detail-oriented and able to understand instructions and work independently.</li>
</ul>
Best-in-Class Benefits and Perks
We value our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:
<ul>
<li>Comprehensive health coverage: Medical, dental, and vision insurance provided</li>
<li>Robust retirement planning: 401(k) plan available with employer matching</li>
<li>Financial security: Life and disability insurance for added protection</li>
<li>Flexible financial options: Health savings and flexible spending accounts offered</li>
<li>Well-being and work-life balance: Generous vacation time, paid holidays</li>
</ul>
Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.
More about The START Center for Cancer Research
Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world. Learn more at STARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Administrative Research Assistant

<h3>Job Description</h3>
Job Description
The Development Scientist will support microbiological lab activities for antimicrobial susceptibility testing (AST). The incumbent performs experiments as defined and planned by supervisor; reviews test results for experimental error and determines if repeats are required. Updating project lead(s) with data and any issues will be required, as well as an ability to work in cross-functional teams. Position Requirements: Bachelor's degree in a Life Science or related field with 1+ years experience in laboratory experience. Strong communication skills with the ability to work in a multidisciplinary team environment. Ability to problem solve is a must. Knowledge of aseptic lab techniques, pipetting, good laboratory practice (GLP), good documentation practices (GDP), and general wet bench experience. Ability to be flexible and work in a rapidly changing task environment and with variety of tasks. Familiarity with Excel and data analysis is desired.
Company DescriptionNicman Group is a consulting company that has a blend of internal and external projects. This isn't a staffing augmentation position, but rather one where you will be joining an existing NIcman team on a long-term project. 
<h3>Company Description</h3>
Nicman Group is a consulting company that has a blend of internal and external projects. This isn't a staffing augmentation position, but rather one where you will be joining an existing NIcman team on a long-term project.

Development Scientist I

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
The Summer Intern, Agentic Systems will support discovery research at Arrowhead Pharmaceuticals by contributing to the development of advanced AI systems that assist scientific research and decision-making. This internship offers hands-on experience building and testing AI-driven tools that support data exploration, evidence synthesis, and hypothesis generation in a collaborative research environment. The intern will work alongside computational and scientific teams to explore how autonomous AI systems can accelerate research workflows and support therapeutic discovery.
This is an 11-week Summer Internship Program paying $27.00 per hour and requires full-time, on-site work five days per week at the designated location.
Responsibilities
<ul>
<li>Support the design and development of AI-driven systems that assist with research analysis and scientific reasoning.</li>
<li>Contribute to building and testing autonomous or semi-autonomous AI workflows that integrate data from multiple sources.</li>
<li>Assist with literature review, data retrieval, and evidence synthesis using AI-enabled tools.</li>
<li>Help develop summaries, visualizations, or reports that communicate insights generated by AI systems.</li>
<li>Collaborate with computational and scientific team members to refine workflows and improve usability.</li>
<li>Participate in testing, iteration, and evaluation of AI systems to improve performance and reliability.</li>
<li>Present progress updates and findings during team meetings.</li>
<li>Support documentation and knowledge-sharing related to AI tools and workflows.</li>
</ul>
Requirements
<ul>
<li>Currently pursuing a PhD in Computer Science, Computational Biology, Bioinformatics, Data Science, or a related quantitative field.</li>
<li>Proficiency in Python, with experience building analytical pipelines or AI-driven applications.</li>
<li>Familiarity with large language models (LLMs) or AI-based automation tools.</li>
<li>Basic understanding of biological or biomedical research concepts.</li>
<li>Strong problem-solving and analytical skills.</li>
<li>Excellent verbal and written communication skills.</li>
<li>Ability to collaborate effectively in a cross-functional research environment.</li>
<li>Excellent verbal and written communication skills and ability to collaborate in a cross-functional research environment.</li>
</ul>
Preferred 
<ul>
<li>Experience working with agent-based or multi-step AI workflows.</li>
<li>Familiarity with API integration and external data sources.</li>
<li>Exposure to scientific or biomedical data platforms.</li>
<li>Experience creating dashboards, reports, or automated summaries.</li>
<li>Strong interest in applying AI to scientific research or drug discovery.</li>
</ul>
California pay range $11,440—$11,440 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
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