URGENTLY HIRING: Research Associate I

Research Associate I u2013 Translational Biology INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP AN IMMEDIATE PHONE INTERVIEW ufeff Job Description This Research Associate I role in Translational Biology focuses on clinical research support in a GCP/GLP environment, with a strong emphasis on clinical sample management, sample logistics, and coordination across internal teams and external partners. The position supports translational biology efforts for advanced therapeutic programs, including cell and gene therapy, and involves managing clinical and pre-clinical samples, maintaining documentation and databases, and contributing to high-quality laboratory operations and data integrity. Responsibilities + Provide research and operational support for translational biology efforts across cell and gene therapy, RNA, siRNA, and gene editing programs. + Facilitate clinical sample logistics and support clinical sample reconciliation, ensuring accurate paper and electronic record keeping. + Manage and oversee the clinical sample management process, including the development and implementation of a centralized database for clinical samples and consent tracking. + Perform day-to-day sample and database management, ensuring data accuracy, completeness, and traceability. + Assist with coordination, distribution, and tracking of clinical trial supplies to domestic and international biopsy, surgical, and laboratory sites. + Ensure compliance with GCP and GLP guidelines, as well as FDA regulations and ICH guidelines, in all aspects of sample handling and documentation. + Maintain training manuals, materials, and resources for clinical trial biopsy sites, and support distribution of training materials related to sample management. + Collaborate closely with Clinical Operations, Data Management, Biostatistics, and external vendors to support data transfer and analysis needs. + Support communications and build productive relationships with key stakeholders, including CROs, specialty laboratory vendors, and external collaborators. + Work with Laboratory Operations and Sample Management teams to track and reconcile incoming sample shipments across various clinical and pre-clinical studies. + Assist laboratory teams in writing, reviewing, and updating SOPs, reports, and publications related to clinical analyses. + Assist with tracking and reporting departmental metrics as applicable, contributing to continuous improvement of processes. + Exercise discretion and sound judgment in handling confidential information and ensure strict adherence to all relevant regulatory and quality standards. + Contribute to a collaborative, fast-paced team environment and actively participate in problem solving and process optimization. Essential Skills + Bacheloru2019s degree in Biology, Biochemistry, or a related field. + At least 2 years of hands-on clinical sample management or clinical research operations experience in a biotech or healthcare setting. + Demonstrated experience working in a GCP/GLP environment. + Strong technical proficiency and high-quality sample handling with strict adherence to laboratory SOPs. + Ability to exercise discretion and judgment in handling confidential information. + Working knowledge of and adherence to FDA regulations, ICH guidelines, and GCP in daily tasks. + Strong organizational skills with the ability to balance and prioritize changing demands. + Proven track record of effective teamwork and collaboration in cross-functional settings. + Ability to communicate clearly across multiple parties and functional groups, including external stakeholders. + Excellent technical writing skills, with the ability to articulate complex technical concepts to diverse audiences. + Demonstrated problem-solving skills and the ability to address complex issues in a structured and timely manner. Additional Skills & Qualifications + BG in biology, virology, molecular biology, or related scientific disciplines. + Hands-on experience with PCR, ELISA, and other molecular biology techniques. + Experience with animal research and working with AAV (adeno-associated virus) is highly beneficial. + Experience supporting cell and gene therapy, RNA, siRNA, or gene editing programs. + Experience in clinical sample logistics, including international site support and vendor coordination. + Ability to develop new training materials and procedures for sample management and site operations. + Comfort working in a dynamic, fast-paced environment with a strong desire to contribute to innovative medicines that improve patientsu2019 lives. Work Environment The role is primarily based in a laboratory environment within a modern, state-of-the-art facility focused on cell and gene therapy. The Research Associate will spend most of the day working in the lab, including work with animals and handling biological samples, and will also spend some time at a desk performing documentation, database management, and communication tasks. The environment is fast-paced and collaborative, with close interaction among laboratory teams, clinical operations, data management, biostatistics, and external partners. Standard laboratory safety procedures and appropriate lab attire and personal protective equipment are required while working in the lab. Job Type & Location This is a Contract position based out of Columbus, OH. Pay and Benefits The pay range for this position is $25.00 - $27.00/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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on May 25, 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 process due to a disability, please email for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Created: 2026-05-13