Clinical Data Manager

Proclinical; Boston (MA); Remote; USD 83,000 - 131,000; Full time

Job summary

Proclinical is seeking a Clinical Data Manager to join our Clinical Data Management team supporting studies in the rare disease and pharmaceutical space. This contract role offers remote work for US-based candidates and the opportunity to contribute to groundbreaking research that impacts patients worldwide.

The successful candidate will act as the primary data management contact, coordinate with CROs and study teams, ensure data quality, and oversee data validation, coding, and documentation in

Qualifications

• Bachelor's degree in mathematics, science, or related field.
• Experience in clinical data management within biotechnology, pharmaceuticals, or 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.

Responsibilities

• 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.

Skills

Clinical data management

CRO coordination

Regulatory compliance

Data validation

Project teamwork

Communication skills

Genetics

Oncology

Ophthalmology

Education

Bachelor's degree in mathematics, science, or related field

Job description

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.