Clinical Office Coordinator
GForce Life Sciences, Minneapolis, MN, United States
Consultant, Clinical Office Coordinator, Medical Devices
Summary
Our client,
a leading global medical device company,
has engaged GForce Life Sciences to provide a Clinical Office Coordinator. The coordinator will support ongoing clinical research activities. This is a great opportunity for someone looking to break into the clinical research field, as the role is highly trainable and offers exposure to study operations within a well-established and supportive team.
Responsibilities
Perform daily review and maintenance of clinical compliance data, including verifying physician credentials and license status
Support administrative aspects of clinical studies to ensure accuracy and regulatory compliance
Maintain organized and up-to-date documentation related to study activities
Assist with additional tasks and responsibilities as study needs increase
Collaborate with internal team members to support overall study execution
Requirements
Strong attention to detail and ability to manage repetitive tasks with accuracy
Proactive mindset and willingness to take on additional responsibilities
Nice to Have
Associate’s or Bachelor’s degree (or currently pursuing)
Interest in clinical research, healthcare, or medical devices
Terms & Start
12+ month contract
Hybrid in Hennepin County, MN
Benefits included (Medical, Dental, Vision)
#J-18808-Ljbffr
Summary
Our client,
a leading global medical device company,
has engaged GForce Life Sciences to provide a Clinical Office Coordinator. The coordinator will support ongoing clinical research activities. This is a great opportunity for someone looking to break into the clinical research field, as the role is highly trainable and offers exposure to study operations within a well-established and supportive team.
Responsibilities
Perform daily review and maintenance of clinical compliance data, including verifying physician credentials and license status
Support administrative aspects of clinical studies to ensure accuracy and regulatory compliance
Maintain organized and up-to-date documentation related to study activities
Assist with additional tasks and responsibilities as study needs increase
Collaborate with internal team members to support overall study execution
Requirements
Strong attention to detail and ability to manage repetitive tasks with accuracy
Proactive mindset and willingness to take on additional responsibilities
Nice to Have
Associate’s or Bachelor’s degree (or currently pursuing)
Interest in clinical research, healthcare, or medical devices
Terms & Start
12+ month contract
Hybrid in Hennepin County, MN
Benefits included (Medical, Dental, Vision)
#J-18808-Ljbffr