Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Medical Affairs Associate

Job

Dawar Consulting, Inc.

Remote

$74,880 Salary, Full-Time

Posted 2 weeks ago (Updated 3 days ago) • Actively hiring

Expires 8/3/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
100
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Medical Affairs Associate Dawar Consulting, Inc. Santa Monica, CA Job Details Contract $36 an hour 23 hours ago Benefits Health insurance Dental insurance 401(k) Vision insurance Paid sick time Qualifications Project team coordination Operations coordination Research project coordination ICH guidelines Clinical research compliance Bachelor's degree Project stakeholder communication Full Job Description Our client, a world leader in biotechnology and life sciences, is seeking a " Medical Affairs Associate (Hybrid) ".
Duration:
Long-Term Contract (Possibility Of Further Extension)
Pay Rate:
$36/hr on W2
Company Benefits:
Medical, Dental, Vision, Paid Sick Leave, 401
K Job Summary:
In this role, you will support expanded access programs, single-patient IND requests, and clinical study operations. You will coordinate program activities, manage timelines and documentation, communicate with investigators, sites, CROs, and vendors, and ensure compliance with regulatory and company requirements.
Responsibilities:
Support Medical Affairs and clinical program activities Coordinate expanded access and single-patient IND processes Track study milestones, timelines, and deliverables Manage vendor and CRO communications Review study and regulatory documentation Prepare status reports and support issue resolution Collaborate with cross-functional teams and clinical sites
Requirements:
BS/BA/RN
in Life Sciences, Nursing, or related field 3-5 years of clinical research, clinical operations, or medical affairs experience Knowledge of ICH-GCP and clinical trial processes Strong project coordination and communication skills Oncology, hematology, or cell therapy experience preferred Medidata
RAVE/EDC
experience is a plus If interested, please share your updated resume at /