Senior Clinical Data Manager

Position: Senior Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $90,000 to $100,000 We are seeking an experienced Senior Clinical Data Manager to lead and oversee data management activities across clinical trials while ensuring the integrity, accuracy, and reliability of clinical data. This role is responsible for managing all phases of clinical data management, including study start-up, CRF design, database set‑up, edit check specifications, vendor oversight, data cleaning, and database lock activities, while maintaining compliance with GCP, CDISC standards, regulatory requirements, and company SOPs. The ideal candidate will serve as Lead Data Manager for assigned studies, coordinating resources, managing timelines and deliverables, collaborating with internal teams, sponsors, and vendors, and supporting audits and inspections. The Senior Clinical Data Manager will also contribute to process improvements, mentor team members, and provide risk management guidance to ensure high‑quality project execution aligned with client expectations. Responsibilities: Ensure the integrity, reliability, and accuracy of clinical trial data. Maintain clinical data quality and consistency in line with regulatory requirements, SOPs, processes, and data standards. Verify external data conforms to data transfer specifications. Ensure all data management activities comply with GCP, regulatory requirements, and Pharmaron Clinical/Sponsor SOPs. Apply CDISC or applicable standards to data/database programming throughout the trial. Adhere to Pharmaron Clinical policies and procedures. Act as Lead Data Manager for clinical trials: arrange resources, assess workload, define study scope, and create timelines. Oversee all data management tasks for assigned trials; monitor deliverables to meet timelines and quality standards. Participate in internal/external meetings, audits, and regulatory inspections. Communicate effectively with internal teams, vendors, and clients; provide risk management assessments. Mentor and train team members; perform data management tasks as needed. Lead project teams to deliver services aligned with client needs and contractual obligations. Develop and improve clinical data management SOPs and processes; recommend improvements to senior management. What We’re Looking For: Bachelor’s Degree with at least 4 years’ experience within a data management role, understanding of processes including study management, vendor management, CRF design, database set‑up, edit check specification, DMPs, and data cleaning activities up to and including database lock. Demonstrated knowledge of the functions and activities of clinical trials. Demonstrated knowledge of GCP and other regulatory requirements for clinical trials. Benefits: Insurance including Medical, Dental & Vision with significant employer contributions Employer‑funded Health Reimbursement Account Healthcare & Dependent Care Flexible Spending Accounts 100% Employer‑paid Employee Life and AD&D Insurance, Short‑ and Long‑Term Disability Insurance 401k plan with generous employer match Access to an Employee Assistance Program As an Equal Employment Opportunity and affirmative action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences. #J-18808-Ljbffr