Life Science Jobs at Emmes Group | CDM Role | Apply Now
Are you looking for Life Science Jobs in clinical research? Emmes Group Careers presents an exciting opportunity for experienced professionals to join as a Clinical Data Manager (CDM) in Bengaluru, India. If you have expertise in Clinical Data Management, EDC systems, regulatory compliance, and clinical trial operations, this CDM Jobs opportunity could be the ideal next step in your career. Explore the responsibilities, qualifications, and requirements below and apply to become part of a globally recognized clinical research organization.
About Emmes Group
Emmes Group is a leading clinical research organization with more than 47 years of scientific excellence. The company specializes in advancing research across cell and gene therapy, vaccines, infectious diseases, ophthalmology, neuroscience, and rare diseases. Through its full-service CRO capabilities and innovative technology solutions under Veridix AI, Emmes Group is transforming clinical trials and helping accelerate the development of life-changing therapies worldwide. The organization is committed to fostering a culture of integrity, innovation, collaboration, and global health impact.
Job Overview
- Position: Clinical Data Manager (CDM)
- Location: Bengaluru, India
- Department: Clinical Operations
- Job Type: Regular Full-Time
Key Responsibilities
- Develop and maintain data management plans (DMPs), data validation specifications, and other study-related documents.
- Design and review CRFs/eCRFs in collaboration with clinical teams and vendors.
- Oversee the setup, validation, and ongoing maintenance of electronic data capture (EDC) systems, including Medidata Rave, Oracle InForm, Veeva, and REDCap.
- Perform and review data cleaning, query generation, and issue resolution activities.
- Ensure timely and accurate database lock and data delivery to biostatistics and other stakeholders.
- Coordinate with CROs, EDC vendors, and central laboratories to ensure timely and compliant data activities.
- Liaise with internal teams, including clinical, regulatory, biostatistics, and safety to ensure alignment of data deliverables with study goals.
- Participate in study team meetings and contribute to project timelines and risk management.
- Ensure compliance with regulatory requirements, including FDA 21 CFR Part 11 and ICH GCP.
- Conduct or support audits, data review meetings, and internal quality checks.
- Maintain accurate and complete documentation for inspection readiness.
- Perform other duties as assigned.
- Comply with all policies and standards.
Qualifications
Required Qualifications
- Bachelor’s Degree in Life Sciences, Health Information Management, Computer Science, or a related field.
Preferred Qualifications
- Master’s Degree in Life Sciences, Health Information Management, Computer Science, or a related field.
Experience Required
- 3 years of experience in Clinical Data Management (pharmaceutical, CRO, or biotech experience preferred).
- 1–3 years of prior experience with EDC systems and CDISC standards (SDTM/ADaM) preferred.
Skills Needed
- Proficiency in EDC systems such as Medidata Rave, Veeva, and InForm.
- Familiarity with data standards, including CDISC, MedDRA, and WHODrug.
- Experience with database lock processes, query management, and edit checks.
- Knowledge of SAS, SQL, or other data handling languages is a plus.
- Strong attention to detail and organizational skills.
- Excellent communication and interpersonal abilities.
- Ability to manage multiple projects and deadlines.
- Team-oriented mindset with proactive problem-solving skills.
If you are seeking Life Science Jobs in clinical research and data management, this opportunity through Emmes Group Careers is an excellent chance to advance your professional journey. Apply today for these exciting CDM Jobs and become part of a team dedicated to driving innovation and excellence in global clinical research.
