Medical Affairs Associate (100% Remote) - West Coast Preferred

Dawar Consulting, Inc.

Remote, United States

Posted

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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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