Global medical technology leader Stryker is currently hiring a Staff Clinical Data Manager in Bengaluru, India. This opportunity is ideal for professionals with 5+ years of experience in clinical data management, EDC systems, CRF design, and clinical trial data quality management.
The role offers the chance to work in a hybrid environment, collaborating with cross-functional clinical teams to ensure high-quality clinical trial data and regulatory compliance. If you have experience in GCP guidelines, CDISC standards, SAS/SQL, and EDC platforms, this position provides an excellent opportunity to grow within a leading medical device and clinical research organization.
Clinical Data Management professionals seeking roles in clinical trials, CROs, pharmaceutical companies, and medical device companies will find this role particularly valuable for advancing their careers.
Job Details
Position: Staff Clinical Data Manager
Company: Stryker
Location: Bengaluru, India
Work Model: Hybrid
Employment Type: Full-time, Permanent
Industry: Medical Devices / Biotechnology / Clinical Research
Key Responsibilities
The Staff Clinical Data Manager will play a critical role in ensuring clinical trial data integrity, accuracy, and regulatory compliance. Key responsibilities include:
- Develop and maintain clinical data management documentation, including study protocols, CRFs, and Data Management Plans (DMP).
- Design Case Report Forms (CRFs) and configure Electronic Data Capture (EDC) systems for clinical studies.
- Perform data entry, data cleaning, discrepancy management, and query resolution.
- Conduct data validation checks and implement quality control procedures.
- Review clinical data received from vendors and external modules used in clinical trials.
- Develop and execute Standard Operating Procedures (SOPs) related to data management activities.
- Generate data listings, summaries, and reports for clinical study reports.
- Collaborate with clinical operations, biostatistics, and regulatory teams to resolve data issues.
- Ensure compliance with ICH-GCP guidelines, CDISC standards, and regulatory requirements.
- Support the development and validation of clinical data management software tools.
Required Qualifications
Candidates applying for this Clinical Data Manager job in Bengaluru should meet the following criteria:
Basic Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a healthcare-related field
- Minimum 5 years of experience in clinical data management
- Experience working in pharmaceutical, CRO, or medical device industries
- Strong understanding of:
- Clinical trial processes
- Data management principles
- Regulatory guidelines (ICH-GCP)
Technical Skills
Candidates should have experience with:
- Electronic Data Capture (EDC) systems
- CRF design and clinical database setup
- SAS, SQL, or Oracle Clinical
- Clinical trial data validation and quality checks
- CDISC standards
Preferred Qualifications
The following qualifications will be advantageous:
- CCDM certification (Certified Clinical Data Manager)
- Experience with SDTM and ADaM data standards
- Familiarity with FDA / CFR regulations
- Knowledge of data privacy regulations such as GDPR
- Understanding of clinical trial design and regulatory submissions
- Strong communication and cross-functional collaboration skills
Benefits of Working at Stryker
Working at Stryker provides several professional and personal benefits:
- Hybrid work flexibility
- Opportunities to work with global clinical trials and medical device innovations
- Exposure to advanced clinical data management technologies
- Career growth in a leading global healthcare company
- Competitive compensation and employee benefits
How to Apply
