Project Coordinator, Data Monitoring - Entry Level

Medpace; Greater London; On-site; GBP 24,000 - 32,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

PTO

WFH after training

Social events

Competitive pay

Job summary

Medpace is seeking an Entry Level Project Coordinator for our Global Internal Data Monitoring team. This full-time, office-based role supports a collaborative group responsible for safety data review across trials and works with study teams to ensure timely, accurate documentation.

The position offers extensive onboarding and on-the-job training, with a clear path to develop expertise in data monitoring, clinical operations coordination, and project support.

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 of 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

Job description

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. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

At Medpace, Project Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

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 of 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 l-lV 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. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

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.
• Leadership throughout Medpace is both accessible and approachable

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
• 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
• 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.