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Clinical Data Manager

Remote / Online - Candidates ideally in
Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Proclinical
Remote/Work from Home position
Listed on 2026-10-16
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60 - 95 USD Hourly USD 60.00 95.00 HOUR
Job Description & How to Apply Below

Clinical Data Manager - Contract - Remote, US

Looking for an opportunity where your clinical data management expertise can directly support groundbreaking pharmaceutical research?

Proclinical is seeking a Clinical Data Manager to join our Clinical Data Management team supporting clinical studies in the rare disease and pharmaceutical space.

Primary Responsibilities:

The successful candidate will play a key part in ensuring clinical data is accurate, compliant, and ready for analysis. You will collaborate with vendor project managers, clinical data managers, CROs, and cross-functional study teams to maintain high-quality data standards. This is an exciting opportunity to contribute to impactful projects that make a meaningful difference to patients worldwide.

Skills & Requirements:
  • Bachelor's degree in mathematics, science, or a related field.
  • Experience in clinical data management within biotechnology, pharmaceuticals, or a health-related industry.
  • Strong ability to coordinate and manage CRO data managers and project teams, ensuring adherence to policies and procedures.
  • Solid understanding of data management processes, database validation, and regulatory compliance.
  • Excellent collaboration, organizational, and communication skills.
  • Preferred experience in genetics, oncology, and/or ophthalmology.
The Clinical Data Manager's responsibilities will be:
  • Act as the primary data management contact for assigned studies, representing the function on project teams and partnering with CROs.
  • Coordinate and lead clinical data management activities in alignment with company SOPs, policies, and regulatory requirements.
  • Oversee CRO data clean-up from study start-up through data archiving to ensure data quality and integrity.
  • Manage medical coding, data validation checks, database snapshots, and provide data for analysis.
  • Create and maintain study documentation, including the Data Management Manual, CRF completion guidelines, and validation specifications.
  • Design and modify CRFs, and oversee the build, testing, and validation of clinical databases.
  • Prepare and distribute project status reports to project teams and management.
  • Lead the data management team in ensuring databases are validated and ready for transfer and analysis, while supporting standardization of outsourcing partner processes.
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