Senior Clinical Database Programmer

🔥 0 minutes ago

🇮🇳 India – Remote

⏳ Contract/Temporary

🟠 Senior

🖥 Software Engineer

👻 Ghost score 10%

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Lead and supervise the design, implementation, and maintenance of electronic data capture (EDC) and clinical database management systems (CDMS) • Create, implement, and maintain consistency checks and edit checks • Provide technical leadership and mentorship to programming teams and project staff • Serve as the primary technical contact and liaison with sponsors, data management leaders, and cross-functional teams • Manage database lock/unlock procedures and approve database changes • Maintain technical and regulatory documentation, including deviation logs and traceability records • Support integration and programming of CTMS, safety systems, and coding systems • Develop and implement project-specific tools and standards to improve efficiency • Participate in bid defense meetings and provide technical support for new business opportunities • Contribute to study operations from planning through closeout while ensuring regulatory compliance, data accuracy, and system optimization

🎯 Requirements

• 6 to 7 years of experience in clinical data programming • Proficiency in at least one programming environment (e.g., SAS, CDMS, EDC, SQL, VB, Java) • Strong knowledge of SOPs, guidelines, work instructions, SDLC methodologies, ICH-GCP, and applicable regulatory requirements including 21 CFR Part 11 • Demonstrated experience in the clinical research industry or similar regulated environment • Strong communication, organization, and problem-solving skills with proven ability to work independently and collaboratively • Bachelor's degree in relevant science discipline or equivalent work experience (preferred) • Certification in at least one clinical systems platform (e.g., Inform, RAVE, DataLabs, Medrio, Veeva) (preferred) • Experience with multiple systems used in clinical trial processes (e.g., CTMS, medical safety reporting systems, or additional EDC platforms) (preferred) • Presentation skills and experience supporting business development activities (preferred)

🏖️ Benefits

• 6-month contractual assignment • Flexibility and growth opportunities • Continuous learning opportunities • Career paths and opportunities to expand skills across clinical research