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Thermo Fisher Scientific Hiring for Clinical Data Management (CDM), Clinical Programming, and Programmer Analyst

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Thermo Fisher Scientific is hiring for multiple Clinical Data Management (CDM), Clinical Programming, and Programmer Analyst positions in Bengaluru, India. These hybrid opportunities are ideal for candidates from Pharmacy, Life Sciences, Biostatistics, Computer Science, and related backgrounds looking to build a career in clinical research, clinical data management, SAS programming, and bioinformatics.

The company is currently recruiting for the following positions:

  • Clinical Data Assoc II
  • Senior Clinical Data Associate
  • CDM Programmer I
  • CDM Programmer II
  • Programmer Analyst

These openings offer excellent exposure to global clinical trials, GCP-compliant data management, database programming, SAS programming, and cross-functional collaboration with international pharmaceutical and biotech companies.


Available Job Roles at Thermo Fisher Scientific

1. Clinical Data Assoc II

Location: Bengaluru, India
Work Mode: Hybrid
Shift: Second Shift (Afternoons)
Experience: Around 6 Years Preferred

Key Responsibilities

  • Identify and resolve clinical data discrepancies
  • Generate and track data clarification queries
  • Review clinical data listings for consistency and accuracy
  • Perform SAE and vendor reconciliations
  • Support clinical database updates
  • Analyze data validation reports

Required Skills

  • Strong understanding of GCP guidelines
  • Clinical trial terminology knowledge
  • Excellent analytical and communication skills
  • Ability to manage confidential clinical data
  • Strong attention to detail

2. Senior Clinical Data Associate

Location: Bengaluru, India
Work Mode: Hybrid
Experience: 0โ€“2 Years

Key Responsibilities

  • Support database setup and DVM creation
  • Perform data cleaning and query management
  • Review listings and validate clinical trial data
  • Train and guide junior team members
  • Contribute to process improvements

Eligibility Criteria

  • Bachelorโ€™s degree or relevant qualification
  • Knowledge of clinical data management
  • Good problem-solving and communication skills
  • Understanding of medical and clinical terminology

This role is highly suitable for freshers and early-career professionals interested in Clinical Data Management jobs in India.


3. CDM Programmer I

Location: Bengaluru, India
Work Mode: Hybrid
Experience: 0โ€“2 Years

Key Responsibilities

  • Design, build, and test clinical databases
  • Develop edit checks and data validation programs
  • Import and review clinical trial data
  • Create listings for data review
  • Support multidisciplinary project teams

Skills Required

  • Knowledge of programming languages or RDBMS
  • Database development understanding
  • Strong organizational and analytical skills
  • Familiarity with GCP and SOPs

Candidates with skills in SQL, SAS, database systems, or clinical programming can benefit from this opportunity.


4. Programmer Analyst

Location: Bengaluru, India
Work Mode: Hybrid
Experience: Minimum 2 Years

Major Responsibilities

  • Create and validate SAS programs
  • Analyze clinical trial datasets
  • Generate tables, listings, and figures
  • Support bioinformatics and statistical programming activities
  • Work with multidisciplinary research teams

Educational Qualification

  • Bachelorโ€™s or Masterโ€™s degree in:
    • Computer Science
    • Statistics
    • Biostatistics
    • Mathematics
    • Related fields

Technical Skills

  • SAS programming
  • Relational database systems
  • Clinical data analysis
  • Bioinformatics programming

This is an excellent opportunity for professionals seeking SAS Programmer jobs in Clinical Research.


5. CDM Programmer II

Location: Bengaluru, India
Work Mode: Hybrid
Experience: Around 2 Years

Key Responsibilities

  • Build and validate project databases
  • Perform advanced programming support
  • Lead simple to moderate complexity studies
  • Work on process improvement initiatives
  • Manage timelines and programming deliverables

Preferred Technical Skills

  • SAS
  • SQL
  • Crystal Reports
  • JReview
  • Clinical database systems

Candidates with Clinical Data Management programming experience and knowledge of database tools are encouraged to apply.


Why Join Thermo Fisher Scientific?

Thermo Fisher Scientific is one of the worldโ€™s leading life sciences organizations supporting top pharmaceutical companies and biotechnology firms globally.

Benefits of Working at Thermo Fisher Scientific

  • Global clinical research exposure
  • Hybrid work environment
  • Career growth opportunities
  • Collaborative international teams
  • Training and professional development
  • Work on innovative clinical trials across 100+ countries

Who Can Apply?

Candidates from the following backgrounds may apply:

  • B.Pharm
  • M.Pharm
  • Pharm.D
  • Life Sciences
  • Biotechnology
  • Computer Science
  • Statistics
  • Biostatistics
  • Mathematics
  • Clinical Research
  • Bioinformatics
RoleExperience Required
Clinical Data Assoc IIAround 6 years of relevant experience
Senior Clinical Data Associate2 years
CDM Programmer I0โ€“2 years
Programmer AnalystMinimum 2 years
CDM Programmer IIAround 2 years

How to Apply?

Application Link For Clinical Data Assoc II

Application Link For Senior Clinical Data Associate

Application Link For CDM Programmer I

Application Link For CDM Programmer II

Application Link For Programmer Analyst

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