FAQs
What are the responsibilities of an Entry Level Study Start-Up Coordinator?
An Entry Level Study Start-Up Coordinator is responsible for assisting with regulatory submissions, preparing essential study documents, collaborating with internal teams, and supporting the study start-up process for clinical trials at Medpace.
What qualifications are required for this role?
This position is entry level, so no prior experience is necessary. However, candidates should have a Bachelor's degree in a related field and a strong desire to learn and grow in the clinical research industry.
What training opportunities are available for Entry Level Study Start-Up Coordinators?
Medpace provides a robust training program for new employees to build a foundation in industry knowledge and develop their skills. Entry Level Study Start-Up Coordinators will have the opportunity to learn from experienced team members and participate in ongoing training sessions.
How does an Entry Level Study Start-Up Coordinator contribute to the clinical trial management process?
Entry Level Study Start-Up Coordinators play a key role in the study start-up process by assisting with regulatory submissions, document preparation, and collaboration with internal teams. Their contributions help ensure that clinical trials are set up for success from the beginning.
What opportunities for growth and development are available for Entry Level Study Start-Up Coordinators at Medpace?
Medpace values employee growth and development. Entry Level Study Start-Up Coordinators have the opportunity to advance their career within the company through continued training, gaining experience in different areas of clinical research, and taking on new responsibilities as they progress in their role.