CDM Programmer 2 (Veeva EDC & CDB) (Mumbai)

As a CDM Programmer II at Thermo Fisher Scientific, you will be part of a diverse and inclusive team that supports top pharmaceutical companies and biotechs in various clinical trials across multiple countries. Your role will involve working with clinical data management systems and programming tools to ensure operational excellence in clinical trials. You will have the opportunity to contribute to database development, data validations, and improving process efficiencies within a multi-disciplinary project team. Key Responsibilities: - Perform tasks within established timelines and departmental procedures - Design, build, and test project databases & edit checks with Veeva EDC - Define and import data into the system - Create and test listings for data review - Act as the lead on studies of simple to moderate complexity - Participate in process improvement initiatives - Adhere to departmental working practice documents and SOPs Qualifications Required: - Bachelor's degree or equivalent with relevant academic/vocational qualification - Previous experience equivalent to 2+ years - Solid written, verbal, and computer skills - Attention to detail and problem-solving skills - Organizational skills with the ability to manage multiple assignments - Basic experience in programming languages or relational database systems - Working knowledge of programming tools such as SAS, SQL, Crystal Reports, and JReview - Demonstrate leadership ability and initiative - Project management skills and ability to interpret company policies Thermo Fisher Scientific values passion, innovation, and commitment to scientific excellence. Joining the team means working in a collaborative environment where your contributions truly make a difference. If you are looking to be part of a global team that delivers tomorrow's breakthroughs, apply today. As a CDM Programmer II at Thermo Fisher Scientific, you will be part of a diverse and inclusive team that supports top pharmaceutical companies and biotechs in various clinical trials across multiple countries. Your role will involve working with clinical data management systems and programming tools to ensure operational excellence in clinical trials. You will have the opportunity to contribute to database development, data validations, and improving process efficiencies within a multi-disciplinary project team. Key Responsibilities: - Perform tasks within established timelines and departmental procedures - Design, build, and test project databases & edit checks with Veeva EDC - Define and import data into the system - Create and test listings for data review - Act as the lead on studies of simple to moderate complexity - Participate in process improvement initiatives - Adhere to departmental working practice documents and SOPs Qualifications Required: - Bachelor's degree or equivalent with relevant academic/vocational qualification - Previous experience equivalent to 2+ years - Solid written, verbal, and computer skills - Attention to detail and problem-solving skills - Organizational skills with the ability to manage multiple assignments - Basic experience in programming languages or relational database systems - Working knowledge of programming tools such as SAS, SQL, Crystal Reports, and JReview - Demonstrate leadership ability and initiative - Project management skills and ability to interpret company policies Thermo Fisher Scientific values passion, innovation, and commitment to scientific excellence. Joining the team means working in a collaborative environment where your contributions truly make a difference. If you are looking to be part of a global team that delivers tomorrow's breakthroughs, apply today.