Clinical Data Manager

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April 25

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Pharmavise Corporation

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Biotechnology • Pharmaceuticals • Healthcare Insurance

Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.

11 - 50 employees

Founded 2013

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. • The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements. • This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution. • Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol. • Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. • Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams. • Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations. • Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). • Manage database lock activities and contribute to the preparation of clinical study reports (CSRs). • Serve as the primary point of contact for data management vendors and oversee their deliverables. • Participate in study team meetings and provide status updates related to data quality and timelines. • Support audit readiness and participate in regulatory inspections when required.

🎯 Requirements

• Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field. • Advanced degree is a plus. • Minimum of 3–5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment. • Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm , Veeva, REDCap). • Strong understanding of ICH-GCP, FDA regulations, and CDISC standards. • Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug). • Excellent organizational, analytical, and problem-solving skills. • Strong communication and collaboration skills across cross-functional teams. • Experience working on global, multi-site clinical trials preferred.

🏖️ Benefits

• paid holidays • Paid Time Off (PTO) policy • medical insurance