Remote Clinical Site Lead for Medical Device Trials

GForce Life Sciences; Boston (MA); On-site; USD 80,000 - 110,000; Part time

Job summary

GForce Life Sciences seeks a Clinical Site Lead for a Fortune 500 Medical Device client. The CSL will oversee site maintenance, data collection, and field monitoring to ensure protocol and GCP compliance, including ADE review and site training.

Responsibilities include resolving data discrepancies, coordinating site initiation, and ensuring timely submission of study documents with 50-75% travel and a 12-month contract. Remote/home-based with preferred Boston-area candidates.

Qualifications

• Bachelor’s degree in a natural science or related field required.
• 3-5+ years of clinical trial monitoring experience required.
• 5-8+ years in medical device clinical trials preferred.
• Experience in a medical device/pharmaceutical company or clinical/hospital environment advantageous.

Responsibilities

• Monitor clinical studies at sites to ensure GCP/regulatory compliance and accurate data collection.
• Review data and source documents for accuracy and completeness; manage data queries.
• Report adverse events and protocol deviations; ensure device complaints/malfunctions are documented.
• Coordinate site initiation, subject enrollment, and monitoring visits; train site personnel.

Skills

Clinical site monitoring

Regulatory compliance

Adverse event review

Data discrepancy resolution

Site initiation & monitoring

Education

Bachelor’s degree in natural science or related field

Job description

GForce Life Sciences seeks a Clinical Site Lead for a Fortune 500 Medical Device client. The CSL will oversee site maintenance, data collection, and field monitoring to ensure protocol and GCP compliance, including ADE review and site training.

Responsibilities include resolving data discrepancies, coordinating site initiation, and ensuring timely submission of study documents with 50-75% travel and a 12-month contract. Remote/home-based with preferred Boston-area candidates.