Life Science Job Opportunity at Medpace | Apply Now
Looking for an exciting life science job in clinical research? Medpace is hiring a Regulatory Submissions Coordinator in Turkey (remote), offering a great opportunity to build a career in clinical operations. This role is ideal for candidates passionate about drug development, regulatory processes, and clinical trials, while working with a global CRO leader.
Job Details
- Job Position: Regulatory Submissions Coordinator
- Location: Turkey (Remote)
- Job ID: 12591
About the Company
Medpace is a full-service clinical contract research organization (CRO). The company provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Its mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach.
Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries. The organization leverages local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. If you are exploring medpace careers or a global clinical operations job, this opportunity is worth considering.
Job Description
Our clinical operations activities are growing rapidly, and we are currently seeking a Regulatory Submissions Coordinator to join our Clinical Operations team in Turkey. This position plays a key role in the clinical trial management process at Medpace.
If you want an exciting life science job where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Please note this would be a remote position in Turkey.
Qualifications
This Life Science Job requires:
- Bachelor’s degree in a Life Sciences field
- Experience preparing, reviewing, and submitting regulatory documentation to Ethics Committees and Regulatory Agencies
- Full professional proficiency in English
- Interest in drug development and clinical trials
- Knowledge of Microsoft® Office
- Excellent organization and communication skills, with great attention to detail
Key Responsibilities
This Life Science Job Role Responsibilities include:
- Prepare, review, and file clinical trial applications
- Communicate with research sites (hospitals, etc.) to collect all essential documents required before the site starts to enrol patients to participate in the clinical trial
- Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration
- Ensure submissions comply with applicable regulations and guidance documents
- Advise on changing country regulations and compliance requirements
- Track submissions and ensure timely filing of documents
Why Medpace Careers?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work done over the past 30+ years has positively impacted the lives of countless patients and families facing hundreds of diseases across key therapeutic areas. The work being done today will improve the lives of people living with illness and disease in the future.
