Senior Clinical Research Project Coordinator - Denver

Medpace; Denver (CO); Hybride; USD 75 000 - 110 000; Plein temps

Avantages offerts par ce poste

Medical insurance

Dental insurance

Vision insurance

401(k)

Vacation

Work from home flexibility

Long-term disability

Short-term disability

Life insurance

Pet insurance

Travel reimbursement

Résumé du poste

Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Denver. You will engage in day-to-day trial management, support the CTM, and coordinate meetings while maintaining accurate status reports and regulatory filing oversight.

Qualifications include a health/life sciences degree and prior pharmaceutical experience, plus strong Excel, organizational, and communication skills.

Qualifications

• Bachelor's degree in health or life sciences field.
• Prior experience as a Study Coordinator or in pharmaceutical industry.
• Strong computer, organizational, and communication skills (MS Office).

Responsabilités

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of tasks with accuracy.
• Compile and maintain project-specific status reports.
• Interact with the Sponsor, study sites, and internal associates.
• Provide oversight and quality control of internal regulatory filing system.
• Manage study supplies.
• Create and maintain project timelines.
• Coordinate project meetings and produce meeting minutes.

Connaissances

Excellent communication

Excellent organization

Excel

Word processing

Databases

Windows

Formation

Bachelor's degree in health or life sciences

Description du poste

Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-basedProject Coordinatorto join our Clinical Trial Management team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic/Renal, Infectious Disease/CNS/Ophthalmology and more. If you are looking for a fast paced, collaborative work environment in clinical research and want to develop your career even further, then this is the opportunity for you. Medpace provides Project Coordinators a 4-6 week training program that incorporates a virtual and hands on learning experience, especially for those without previous clinical research experience.

Responsibilities

• Engage in clinical trial management on a day to day level;
• Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports;
• Interact with the Sponsor, study sites, and internal associates;
• Provide oversight and quality control of our internal regulatory filing system;
• Manage study supplies;
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality meeting minutes.

Qualifications

• Bachelor's degree in a health/life sciences field;
• Prior experience as a Study Coordinator or within the pharmaceutical industry; and
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.

Compensation

A target salary range of $75,000 - $110,000 with potential for bonus awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations).

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.