Entry Level Life Sciences Hiring Event - July 1st at Medpace, Inc.

Leuven, Flemish Brabant, Belgium -

Full Time

Start Date

Immediate

Expiry Date

03 Sep, 26

Salary

0.0

Posted On

05 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Data Validation, Site Monitoring, Project Coordination, Regulatory Submissions, Trial Master File Management, Laboratory Operations, Biomarker Testing, Instrumentation Troubleshooting, Clinical Trial Management, Data Trend Reporting

Industry

Pharmaceutical Manufacturing

Description

Medpace will be hosting an Online Hiring Event targeting Master's students in life sciences. WHEN: July 1st at 11:00 AM You will receive a MS Teams invite to follow the online event. Responsibilities Below are some examples of the positions that we will discuss during the event. Clinical Data Coordinator: Validate entry database designs Report metrics and data trends on projects Identify data conflicts and issues on projects Work with personnel from global research sites to resolve data conflicts Clinical Research Associate Comprehensive training program that provides resources and knowledge to monitor sites independently Travel to non-local, national study sites 60-80% of the time Communicate with medical staff and clinical research physicians on site Project Coordinator - CRO Partner with Clinical Trial Manager to coordinate daily study activities Central point of contact for internal and external team members Create and maintain project timeline Regulatory Submissions Coordinator Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial; Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF); Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards Medical technologist - MRL Perform documentation, and routine lab system operations. Problem solve and work alongside our team of Medical Laboratory Scientists and PhD Scientists to develop and validate new tests and methods for routine and biomarker testing in our expanding laborator. Train on different sets of automated instrumentation to learn maintenance and troubleshooting skills. Qualifications Bachelor's in Life Sciences or related fields Willing to work office-based in Leuven Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Responsibilities

The roles involve coordinating clinical trial activities, validating data, and managing regulatory submissions for research sites. Some positions also require performing laboratory operations and validating new tests for biomarker testing.