Clinical Data Associate

GForce Life Sciences; New Jersey; Remote; USD 70,000 - 90,000; Full time

Job summary

A leading company in life sciences is seeking a Clinical Data Associate II for a 12-month remote contract. The role includes managing biosample activities and ensuring data integrity. Candidates should hold a bachelor's degree in life sciences with at least three years of experience in clinical research. Ideal applicants will demonstrate strong project management skills, data validation expertise, and familiarity with bioanalytical regulations.

Qualifications

• Minimum of 3 years of experience in clinical research, preferably with bioanalysis.
• Familiar with bioanalytical regulations and workflows.
• Experience in working with cross-functional teams.

Responsibilities

• Act as the primary liaison for biosample lifecycle activities.
• Draft and review Data Transfer Agreements (DTAs) and ensure data accuracy.
• Ensure compliance with bioanalytical regulations and company standards.

Skills

Project Management

Communication

Data Validation

Collaboration

Education

Bachelor’s degree in Life Sciences

Tools

Laboratory Information Management Systems (LIMS)

Biosample tracking tools

Job description

Clinical Data Associate II

12-month contract

Remote - EST Hours

Key Responsibilities:

• Act as the primary liaison for BGBR on all biosample lifecycle activities, including metadata tracking and sample reconciliation.
• Draft and review Data Transfer Agreements (DTAs) and other specification documents to ensure accurate biosample data collection, transfer, and reporting.
• Review and validate biosample metadata across multiple datasets (e.g., subject ID, visit name, collection date/time); work with data management, CROs, and laboratories to resolve discrepancies.
• Collaborate cross-functionally with teams in bioanalysis, data management, and statistical programming to streamline workflows and ensure data quality.
• Ensure compliance with bioanalytical regulations and company standards.

Qualifications:

• Bachelor’s degree in Life Sciences or related field.
• Minimum of 3 years of experience in clinical research, preferably within bioanalysis or biomarker operations.
• Familiarity with Laboratory Information Management Systems (LIMS) and biosample tracking tools.
• Experience working in cross-functional teams across multiple departments.
• Strong project management and organizational skills; ability to manage multiple complex projects simultaneously.
• Excellent verbal and written communication skills.
• Solid understanding of bioanalytical regulations and workflows.
• Experience with SDTM standards is a plus.