Spring 2026 Co-Op Early Clinical Development - Hematology, Oncology, and Cell Therapy

Celgene • Princeton, NJ

109d • $27 - $43 • Hybrid

About The Position

The Associate Clinical Scientist/Clinical Science co-op function provides scientific expertise necessary to design and deliver clinical studies and programs in early clinical development. The focus will be on hematology, oncology and cellular therapies. Supports execution of assigned clinical trial activities and works closely with Clinical Scientist to execute activities associated with trial conduct. Supports trial level activities for one or more trials with the necessary supervision. The full-time co-op will take place January - June 2026.

Requirements

• Currently enrolled in an undergraduate or graduate school program and is aspiring a degree in Life Sciences (BS, MS, MD, PhD, PharmD, RN or similar scientific field preferred).
• Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
• Entry level medical writing skills and medical terminology.
• Basic knowledge of disease area, compound, and current clinical landscape.
• Detail-oriented with commitment to quality.
• Critical thinking and problem-solving skills.
• Adaptable/flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism).
• Proficient skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., patient profiles, report generating tools).

Responsibilities

• Assist in the development, review, and amendment of clinical study protocols and related documents (e.g., Informed Consent Forms, Investigator Brochures).
• Support the design and implementation of clinical trials in collaboration with cross-functional teams (e.g., Clinical Operations, Data Management, Regulatory Affairs).
• Conduct literature reviews and contribute to scientific rationale for study design and endpoints.
• Review and interpret clinical data, including safety and efficacy data, and identify trends or issues.
• Draft, review, and edit clinical narratives and other study-related documents.
• Support the development of site and Clinical Research Associate (CRA) training materials.
• Participate in the review and development of Case Report Forms (CRFs) to ensure alignment with protocol requirements.
• Assist with the submission and management of clinical documents in the Trial Master File (TMF).
• Collaborate with medical monitors and other team members to address clinical questions and resolve study-related issues.
• Contribute to the preparation of clinical study reports, regulatory submissions, and responses to health authority queries.
• Ensure compliance with Good Clinical Practice (GCP), company policies, and regulatory requirements.
• Provide regular updates to management and participate in team meetings.

Benefits

• Medical, pharmacy, dental and vision care.
• Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP).
• Financial well-being resources and a 401(K).
• Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support.
• Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility.
• Parental, caregiver, bereavement, and military leave.
• Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
• Other perks like tuition reimbursement and a recognition program.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Industry: Merchant Wholesalers, Nondurable Goods
• Education Level: Bachelor's degree