At a Glance
- Tasks: Coordinate projects and support data monitoring teams to ensure clinical trial success.
- Company: Join Medpace, a leading clinical research organisation with a mission to improve patient outcomes.
- Benefits: Enjoy competitive pay, health benefits, and opportunities for professional growth.
- Other info: Be part of a collaborative culture that values creativity and continuous learning.
- Why this job: Kickstart your career in a dynamic environment with hands-on training and mentorship.
- Qualifications: No prior experience needed; just bring your enthusiasm and willingness to learn.
The predicted salary is between 51750 - 63250 £ per year.
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Entry Level Project Coordinator to join our Global Internal Data Monitoring team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. At Medpace, Project Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field.
Responsibilities
- Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review safety and efficacy data for ongoing trials.
- Act as a liaison between Clinical Operations, Sponsors, and DMC and SAC members.
- Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes).
- Assist in the development and maintenance of study specific documents describing DMC processes and procedures.
- Maintain the study blind and handle unblinded materials with discretion to ensure confidentiality.
TRAVEL: None. Training is available for entry-level candidates.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research.
Why Medpace?
- Purpose-Driven Work: Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.
- Collaborative Culture: Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Continuous Growth & Development: Office based environment with on-site mentors, defined career paths with clear advancement opportunities, industry renowned onboarding and training programs designed to accelerate professional development, ongoing training and continuous learning opportunities throughout your career, and an environment that encourages employees to influence change, contribute ideas, and grow quickly.
Other Employee Benefits: Competitive compensation programs that recognize and reward performance, comprehensive health, wellness, retirement, and PTO benefits, office based culture with occasional WFH that provides flexibility for eligible positions after training, and company-sponsored social events. Please note benefits may vary based on country.
What To Expect Next: A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Project Coordinator, Data Monitoring - Entry Level employer: Medpace
Join our dynamic Clinical Operations team in London, where we prioritise employee growth and foster a collaborative work culture. As a Clinical Trial Site Relationship Coordinator, you'll benefit from ongoing professional development opportunities while working in a vibrant environment that values strategic relationships and innovative solutions in clinical research. Enjoy the unique advantage of reduced travel while making a meaningful impact in the field of clinical trials.
