Medpace

Sr. Clinical Research Project Coordinator (Clinical Research Coordinator Experienced)

Medpace • $75K — $110K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a health/life sciences field
  • Prior experience as a Study Coordinator or in the pharmaceutical industry
  • Strong computer skills including word processing, databases, and Excel
  • Excellent organizational and time management skills
  • Effective verbal and written communication abilities

Responsibilities

  • Engage in daily clinical trial management activities
  • Collaborate with the project CTM to ensure timely task delivery
  • Compile and maintain detailed project status reports
  • Serve as a liaison between Sponsors, study sites, and internal teams
  • Oversee quality control for regulatory filing processes
  • Manage and order study supplies as needed
  • Create and maintain project timelines and meeting schedules

Benefits

  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Flexible work-from-home options
  • Paid vacation and holidays
  • Short-term and long-term disability insurance
  • Health savings and flexible spending accounts
  • Pet insurance and travel expense reimbursement
Full Job Description
Job Summary

Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to 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). Applications will be accepted on an ongoing basis. For more details, please discuss with your recruiter.

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.

About Medpace

Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
Learn more about Medpace
Size
4,700 employees
Market Cap
$6.4 billion
Industry
Net Income
$145.3 million
Founded
1992
5 Year Trend
+22.1%
Revenue
$925.9 million
NASDAQ

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