Clinical Data Manager / Clinical Data Manageress

Clinical Data Manager - Contract - Remote, US

Are you looking for an opportunity to leverage your expertise in clinical data management to support groundbreaking pharmaceutical research? Proclinical is seeking a Clinical Data Manager to join our Clinical Data Management team, focusing on clinical studies in the rare disease and pharmaceutical sectors.

Primary Responsibilities

The successful candidate will play a crucial role in ensuring that 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 the biotechnology, pharmaceuticals, or health-related industries.
• 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 of the Clinical Data Manager

• 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 to ensure that databases are validated and ready for transfer and analysis, while supporting the standardization of outsourcing partner processes.

Apply online using the form below. Please note that only applications matching the job profile will be considered.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.