Clinical Trial Specialist

Our start-up medical device client is adding a Clinical Trial Specialist to support the execution of clinical studies and play a key role in keeping trials moving smoothly from startup through closeout.

This is a great opportunity for someone who enjoys being at the center of clinical operations — partnering with sites, vendors, monitors, and internal teams to ensure studies stay organized, compliant, and on track.

Your role with the company:

• Serve as a key point of contact between internal teams, clinical sites, and vendors

• Coordinate the day-to-day operational aspects of clinical trials in compliance with GCP, GDP, SOPs, and country-specific regulations

• Manage essential study documentation including IRB approvals, informed consents, agreements, regulatory binders, and site personnel records

• Support clinical sites throughout screening and enrollment by answering questions, resolving issues, and keeping communication flowing

• Review and manage study data in EDC, respond to queries, and help ensure timely, accurate case report form completion

• Coordinate adverse event information and ensure proper communication across teams and sites

• Support investigator, study coordinator, and technologist training meetings

• Assist monitoring staff with visit prep, follow-up, and review of monitoring reports

• Help maintain study supplies, materials, and equipment needed to support successful trial execution

What makes this role interesting:

• Highly collaborative role across clinical field teams, monitors, safety, site managers, and vendors

• Opportunity to be deeply involved in the operational side of medical device clinical trials

• Strong visibility and impact on study execution

• Great fit for someone who thrives in a fast-paced, detail-driven environment

Desired Profile:

• Bachelor’s degree in engineering, biology, nursing, physical sciences, or a related field

• 1+ year of experience in clinical or medical affairs within the medical device industry preferred

• Strong understanding of clinical trial regulations, site documentation, and regulatory binder requirements

• Solid knowledge of medical terminology and anatomy

• Strong communication, organization, and problem-solving skills

• Ability to manage multiple priorities and work independently

• Travel up to 20% as needed

This is an excellent opportunity for someone who wants to grow their career in clinical operations and be part of a team supporting meaningful medical device studies.