CDM Programmer I (Rave / Veeva)

CDM Programmer I:

Join Us as a CDM Programmer I Make an Impact at the Forefront of Innovation. We have successfully supported the top 50 pharmaceutical companies and more than 750 Bio-techs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

Role Overview:

Works with clinical data management systems and programming tools to provide programming support in data management activities and deliverables including, but not limited to, database development and data validations. Works within a multi-disciplinary project team to complete assigned tasks on time and within budget.

What Youll Do:

• • Performs tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract.
• • Designs, builds and tests project databases & edit checks.
• • Defines and imports data into the system.
• • Defines, creates and tests listings for data review.
• • Researches and leverages resources to resolve issues and manages simple to moderate tasks through the development and application of new knowledge and/or professional skills.
• • Increases knowledge base and professional skills in areas including programming and technology.
• • Supports a multidisciplinary team and may begin to assist with some lead
• • programming activities with oversight.
• • Ensures adherence to departmental working practice
• • documents and SOPs, and contributes to informal training materials.
  

Education and Experience Requirements:

• Bachelor's degree or equivalent and relevant formal academic
• Previous experience (Min 1 to 1.6 Years) that provides the knowledge, skills, and abilities to perform the job
• Should have experience in RAVE / Veeva EDC

Knowledge, Skills and Abilities:

• • Good written, verbal and computer skills
• • Good attention to detail and problem solving skills
• • Good organizational skills with the ability to adapt and adjust to changing priorities and manage assignments to deadlines
• • Knowledge of one or more programming languages or knowledge of relational database systems (RDBMS) and structure
• • Capable of maintaining a high degree of confidentiality with clinical data and client's proprietary data
• • Capable of attaining, maintaining and applying a working knowledge of GCPs and applicable SOPs
• • Capable of working well with others
• • Demonstrated initiative and motivation
  

Working Conditions and Environment:
• Work is performed in an office or clinical environment with exposure to electrical office equipment.• Occasional drives to site locations. Potential Occasional travel required.

Your Career Growth:

We are hiring a team in India to support our FSP client - a large, globally recognized biopharmaceutical organization with a strong legacy in specialty medicines, vaccines, and scientific innovation. This sponsor is known for its commitment to patients, global research and development, and long-term investment in science. As a client dedicated FSP employee, you will collaborate with our clients global data science team, contribute to complex and high visibility initiatives, and work within a mature FSP delivery model focused on quality and partnership.

Our FSP model supports continuous learning and career development by offering employees tailored learning pathways, stretch assignments, and mentorship this allows FSP professionals to expand their horizons. This role opens multiple career paths. You could progress along the Clinical Data Management track (e.g., CDM Prog I, CDM Prog II,Sr CDM Prog) or transition into Data Standards/Programming, based on skill, impact, and business need.

Why Youll Want to Join:

• Join our FSP Data Management team and help bring lifechanging medicines to patients worldwide. Accelerate your growth with handson experience in modern CDM, from EDC and data quality to AIenabled workflowsbuilding the expertise to lead datadriven study delivery in a rapidly evolving clinical landscape

• Global exposure:

Work on international clinical studies across phases and therapeutic areas, partner with global teams, CROs, vendors, and country operations.

• End-to-end ownership:

Contribute to every stage of study delivery, from set-up to close-out.

• Analytical & project skills:

Strengthen global project management, financial tracking, data analysis, and risk management abilities. Learn new clinical trial technologies like AI platforms to conduct a global clinical trial

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, improving patient diagnostics and therapies or making their laboratory work more efficient, we are here to support them. Our distributed team of more than 90,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com. Thermo Fisher Scientific is a Equal employment opportunity