Medical Affairs Associate (100% Remote) - West Coast Preferred
RemoteUnited StatesUSD 76kmidContractor
- Posted
- today
- Source
- Himalayas
Skills
Communication
Description
Our client, a world leader in biotechnology and life sciences, islooking for a “Medical Affairs Associate (100% Remote)”.
Job Duration: Long Term Contract (Possibility of Extension)
Pay Rate: $36.70/hr on W2
Company Benefits:Medical, Paid Sick leave(asper state policy)
Seeking a Medical Affairs Associate to support clinical operations andMedical Affairs programs, including Expanded Access Programs,Out-of-Specification (OOS) case support, and Single-Patient IND requests. Thisrole will coordinate study activities, vendors, clinical sites, documentation,timelines, and cross-functional deliverables while ensuring compliance withapplicable regulations and procedures.
Key Responsibilities
- Support clinical trials from study start-up through closeout.
- Coordinate Expanded Access Programs, OOS cases, and Single-Patient IND activities.
- Review and maintain essential clinical study documents, including protocols, ICFs, IBs, and CRFs.
- Coordinate CROs, vendors, investigators, and clinical trial sites.
- Track enrollment, screening, data flow, protocol deviations, milestones, and study deliverables.
- Support site feasibility, investigator meetings, site communications, and training.
- Monitor program risks, resolve operational issues, and escalate concerns.
- Prepare study metrics, status reports, newsletters, and management updates.
- Support clinical data queries and database lock activities.
Required Qualifications
- Bachelor's degree in Nursing, Life Sciences, or a related healthcare field.
- 3–5 years of Clinical Operations / Clinical Trial experience.
- Familiarity with CTMS, EDC, and clinical trial documentation.
- Strong organizational, communication, and problem-solving skills.
- Ability to manage multiple priorities in a fast-paced environment.
Preferred Qualifications
- Oncology or Hematology clinical trial experience.
- Cellular therapy experience.
- iMedidata / RAVE EDC experience.
- Study start-up experience in a CRO, sponsor, or site-based regulatory environment.
- Exposure to transplant patient care or apheresis collection.
If interested, please send us your updated resume at
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Originally posted on Himalayas
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