Senior Clinical Research Associate — Remote Trial Operations

Getinge; Waltham (MA); Hybrid; USD 110,000 - 125,000; Full time

Benefits offered by this job

Health insurance

401k plan

Paid Time Off

Tuition reimbursement

Job summary

Getinge is seeking a Senior Clinical Research Associate to oversee randomized clinical studies across solid organ platforms. The role reports to the VP Scientific and Medical Affairs and focuses on data management, site coordination, and ensuring GCP compliance.

The position requires 6+ years in clinical research, a Bachelor's degree, and willingness to travel up to 20%. The role supports diverse teams and contributes to high-quality study deliverables.

Qualifications

• Bachelor's degree in health sciences or related field
• Minimum 6+ years of clinical research associate experience, including randomized trials in medical devices or pharma
• Experience in cardiothoracic clinical trials preferred

Responsibilities

• Provides data coordination and data management for randomized clinical studies.
• Manages investigative site activity for multiple protocols.
• Coordinates budgets and invoicing.
• Creates and implements subject enrollment strategies for assigned sites.
• Ensures trials are conducted per ICH GCP, regulations, and SOPs.
• Designs CRFs/eCRFs for data collection and entry.
• Trains sites on data capture and data cleaning; supports data corrections.

Skills

Data coordination

Data management

Clinical research

Budget coordination

Site management

Travel readiness

Education

Bachelor's degree

Tools

CRF/eCRF design

Data capture tools

Job description

Getinge is seeking a Senior Clinical Research Associate to oversee randomized clinical studies across solid organ platforms. The role reports to the VP Scientific and Medical Affairs and focuses on data management, site coordination, and ensuring GCP compliance.

The position requires 6+ years in clinical research, a Bachelor's degree, and willingness to travel up to 20%. The role supports diverse teams and contributes to high-quality study deliverables.