Remote Medical Affairs Associate – Clinical Ops & Trials

Dawar Consulting

Santa Monica (CA)

Remote

USD 42,000 - 59,000

Full time

2 days ago
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Benefits offered by this job

Medical
Paid Sick leave

Job summary

Dawar Consulting is seeking a Medical Affairs Associate (100% Remote) to support clinical operations and Medical Affairs programs. This role includes coordinating Expanded Access, OOS cases, and Single-Patient IND requests while ensuring regulatory compliance across study activities and cross-functional deliverables.

The position coordinates vendors, clinical sites, documentation, timelines, and data flow from study start-up to closeout.

Qualifications

  • Bachelor's degree in Nursing, Life Sciences, or related healthcare field.
  • 3–5 years of Clinical Operations / Clinical Trial experience.
  • Familiarity with CTMS and EDC systems.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to manage multiple priorities in a fast-paced environment.

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 and CRFs.
  • Coordinate CROs, vendors, investigators, and trial sites.
  • Track enrollment, data flow, protocol deviations, milestones, and deliverables.
  • Monitor risks and elevate concerns; support site communications and training.
  • Prepare study metrics and management updates; assist data queries and lock activities.

Skills

Clinical Operations
Clinical Trials
Strong organizational skills
Communication
Multitasking

Education

Bachelor's degree in Nursing/Life Sciences or related healthcare field

Tools

CTMS
EDC

Job description

Dawar Consulting is seeking a Medical Affairs Associate (100% Remote) to support clinical operations and Medical Affairs programs. This role includes coordinating Expanded Access, OOS cases, and Single-Patient IND requests while ensuring regulatory compliance across study activities and cross-functional deliverables.

The position coordinates vendors, clinical sites, documentation, timelines, and data flow from study start-up to closeout.

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