Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Location: San Francisco, California
Position: Clinical Research Associate
Job ID: 9313
Job Summary:
Medpace is offering a fantastic opportunity for experienced Clinical Research Coordinators (CRCs) to transition into Clinical Research Associate (CRA) roles. With at least one year of CRC experience, you can join Medpace’s growing team, benefit from our PACE® Training Program, and work remotely while earning a competitive salary and generous travel bonus.
What We Offer:
Competitive Travel Bonus
Equity/Stock Option Program
Training Completion and Retention Bonus
Annual Merit Increases
401K Matching
Work from Home: Flexible remote work with customizable hours
Home Office Allowance: Furniture, laptop, mobile phone with internet access
Travel Perks: Retain airline reward miles and hotel points, reimbursement for TSA pre-check, and airline club
Leadership Opportunities: Roles such as Lead CRA, CRA Manager, Clinical Trial Manager, and more
Comprehensive Training: PACE® training program tailored to your experience
International Collaboration: Work with a global team of CRAs
Additional Perks: Access to in-house administrative support and ongoing therapeutic training
Responsibilities:
Site Visits: Conduct qualification, initiation, monitoring, and closeout visits at research sites, ensuring protocol compliance.
Collaboration: Communicate with medical site staff, including coordinators and physicians, to ensure proper trial execution.
Documentation Verification: Verify medical records and source documentation against case report form data, ensuring compliance with regulatory requirements.
Monitoring: Perform risk-based monitoring, including centralized data review, to identify site deficiencies and implement corrective actions.
Compliance: Review regulatory documents, verify medical device/drug accountability, and assess adverse event data reporting.
Recruitment & Retention: Help improve patient recruitment and retention strategies at research sites.
Reporting: Complete monitoring reports and follow-up letters summarizing key findings and corrective actions.
Qualifications:
Education: Minimum of a Bachelor’s degree in a health or science-related field.
Experience: At least 1 year as a Clinical Research Coordinator (CRC).
Travel: Ability to travel 60-70% nationwide (some visits may be remote).
Skills: Proficient in Microsoft Office, with strong communication, presentation, and time management skills.
License: Must maintain a valid driver’s license and the ability to travel to monitoring sites.
Compensation:
Salary: $70,000 - $160,000, based on experience.
Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, work-from-home flexibility, short-term and long-term disability, life insurance, and pet insurance.
Why Medpace?:
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services. With a strong mission to accelerate the development of safe and effective therapeutics, Medpace offers you the chance to work with a globally recognized CRO, impacting patients' lives across key therapeutic areas like oncology, cardiology, CNS, and more.
Perks in San Francisco:
Flexible work environment and competitive PTO (starting at 20+ days)
Employee wellness initiatives and appreciation events
Discounted local business deals
Competitive compensation and growth opportunities
Medpace is proud to be recognized as one of the top workplaces and a leader in the clinical research field.
#LI-Remote
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