Clinical Study Project Specialist, Medical Devices

GForce Life Sciences; Fort Snelling Unorganized Territory (MN); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401k

Job summary

GForce Life Sciences partners with a Fortune 500 Medical Device Company to provide an entry level Consultant, Clinical Project Specialist in the Study Operations Project Management team. This role supports the execution of clinical device studies, ensures adherence to protocol, Good Clinical Practices, and applicable regulatory standards across domestic and international sites.

Key duties include managing committee work, coordinating data entry timelines to sites and labs, and contributing to

Qualifications

• Bachelor's degree in a natural science, pre-medicine, nursing, bioengineering, or related field.
• Minimum 3 years in clinical operations or healthcare-related field; medical training/background beneficial.
• Strong written and verbal communication, interpersonal, presentation, analytical, organizational, and technical writing skills.

Responsibilities

• Manage all aspects of the subject selection committee work.
• Track data entry needs and timelines to sites, core labs, and colleagues.
• Resolve discrepancies with protocol and committee charter requirements.

Skills

Communication skills

Analytical thinking

Organizational skills

Presentation skills

Technical writing

Problem solving

Interpersonal skills

Education

Bachelor's degree in natural science or related field

3+ years in clinical operations or healthcare-related field

Tools

SoCRA certification

ACRP certification

Job description

GForce Life Sciences partners with a Fortune 500 Medical Device Company to provide an entry level Consultant, Clinical Project Specialist in the Study Operations Project Management team. This role supports the execution of clinical device studies, ensures adherence to protocol, Good Clinical Practices, and applicable regulatory standards across domestic and international sites.

Key duties include managing committee work, coordinating data entry timelines to sites and labs, and contributing to