Elevate your clinical research career! Medpace hosts a virtual event on November 18, 2025, for CRCs with 1.5+ years to transition to home-based CRA roles. Join a top CRO for CRA jobs in pharma.
Contents
About the Company
Medpace, Inc., a full-service clinical CRO headquartered in Cincinnati, Ohio, accelerates Phase I-IV trials for biotech, pharma, and medical device sectors worldwide. With 5,000+ employees across 40+ countries, Medpace leverages expertise in oncology, cardiology, CNS, and more, ensuring regulatory compliance and scientific rigor.
Committed to “People. Purpose. Passion.,” the company fosters innovation, structured growth, and a flexible culture, earning accolades like Forbes’ Most Successful Midsize Companies (2021-2024) and Top Workplace 2024.
Job Details
- Company Name: Medpace, Inc.
- Experience: Minimum 1.5 years as Clinical Research Coordinator
- Qualification: Bachelor’s degree in health or science-related field
- Location: United States (home-based; multiple cities including Dallas, New York, Raleigh, Detroit, Los Angeles, San Francisco, Boston, Seattle, Salt Lake City, Missouri)
- Work Type: Home-based (60-70% travel required)
Job Description
Medpace is empowering Clinical Research Coordinators and Research Nurses to advance into dynamic CRA roles through its renowned PACE® Training Program. This virtual networking event spotlights opportunities to conduct monitoring visits, ensure GCP compliance, and support global trials.
Transition to a home-based position with comprehensive training and international collaboration in a risk-based monitoring environment.
Clinical Research Associate (CRA)
- Department: Clinical Operations
- Market: Global Clinical Trials (Biotech, Pharma, Medical Devices)
- Role: Monitor sites, verify data, and ensure protocol compliance in Phase I-IV studies
- Experience: 1.5+ years as CRC/Research Nurse
- Education/Qualification: Bachelor’s in health/science field
Skills/Qualifications
- Proven experience as a Clinical Research Coordinator or Research Nurse
- Valid driver’s license and willingness to travel 60-70% nationwide (some remote visits)
- Proficient in Microsoft Office with strong communication and presentation skills
- Detail-oriented with efficient time management and organizational abilities
- Knowledge of GCP, SOPs, and regulatory requirements
- Ability to verify medical records, adverse events, and site documentation
Key Responsibilities
- Perform qualification, initiation, monitoring, and closeout visits at sites
- Communicate with site staff on protocol adherence and deviations
- Verify investigator qualifications, resources, and eligible subject enrollment
- Review source documentation against case report forms for accuracy
- Conduct risk-based monitoring via integrated Clinical Trial Management System
- Track adverse events, drug accountability, and patient recruitment strategies
- Prepare monitoring reports with findings, deficiencies, and corrective actions
Benefits/Perks
- Competitive travel bonus and equity/stock option program
- Training completion and retention bonuses, plus annual merit increases
- 401K matching and flexible PTO starting at 20+ days
- Home-based work with flexible hours, laptop, mobile hotspot, and furniture allowance
- Retain airline/hotel rewards; in-house travel agents and airline club reimbursement
- Ongoing therapeutic training by in-house physicians and leadership opportunities
- Employee wellness initiatives, appreciation events, and local business discounts
How to Apply
Register for the virtual event by applying through Medpace’s careers portal at www.medpace.com/careers—search for “Virtual CRC Event” or relevant CRA openings. Submit your resume highlighting 1.5+ years CRC experience. Selected candidates will receive Microsoft Teams details.
Verified Post
The post is released by the MedPace LinkedIn page. Click here to visit the post
For more CRA jobs and clinical research jobs, explore Pharma Recruiter. Your CRA journey begins here—apply now and make a difference!
Virtual Networking Event Details
- Date: Tuesday, November 18, 2025
- Time: 6:00 PM to 7:00 PM ET
- Venue: Virtual via Microsoft Teams (details provided upon selection)
- Contact/Email: Apply via careers portal; event format details shared post-selection
Why You Should Join
Medpace cultivates a passionate, purpose-driven culture where CRAs drive therapeutic breakthroughs, impacting patients in oncology, cardiology, and beyond. Enjoy long-term stability with structured paths to Lead CRA or Manager roles, plus global team exposure.
Thrive in a flexible, compliant environment offering continuous training, recognition, and work-life balance—join a CRO that’s transformed lives for 30+ years.
FAQs
Who qualifies for Medpace’s CRA transition via this event?
CRCs or Research Nurses with 1.5+ years experience and a Bachelor’s in health/sciences; 60-70% travel readiness required.
How do I prepare for the virtual networking event?
Update your resume with CRC achievements; expect discussions on monitoring, GCP, and career goals. Event details follow selection.
What does the PACE® Training Program entail for CRA jobs?
Comprehensive home-based training to become a full CRA, including therapeutic education by physicians and risk-based monitoring skills.
What growth opportunities await in Medpace’s clinical research roles?
Leadership tracks like Lead CRA or Trial Manager, plus bonuses, equity, and international projects in a Top Workplace environment.