Thermo Fisher Scientific has announced two new job opportunities in India for professionals interested in clinical research, SAS programming, bioinformatics, and clinical trial feasibility. The latest Thermo Fisher Scientific Jobs 2026 include openings for Programmer Analyst II and Feasibility Site Specialist.

The Programmer Analyst II position is a hybrid, mid-shift opportunity in Bangalore and requires substantial SAS programming experience. In contrast, the Feasibility Site Specialist position is a fully remote India role requiring 0–2 years of relevant feasibility or clinical research experience.

These opportunities are part of Thermo Fisher Scientific and its PPD clinical research business, which supports pharmaceutical, biotechnology, medical device, academic, and government customers across global clinical development.

Thermo Fisher Scientific Job Openings 2026

1. Programmer Analyst II – Hybrid/Mid Shift

Job Requisition ID: R-01354653
Employment: Full-Time
Work Mode: Hybrid
Location: Bangalore, India
Shift: Second Shift / Afternoons

The Programmer Analyst II performs bioinformatics and SAS programming activities supporting statistical and computational requirements of clinical research projects. The professional works within study teams under the direction of a lead programmer and may undertake lead programming responsibilities for selected studies.

Key Responsibilities

• Create, execute, maintain, and validate SAS programs for clinical research projects.
• Transfer and integrate data across different data management systems and operating systems.
• Combine clinical data from multiple sources and structures.
• Generate summary datasets, reports, listings, tables, and figures.
• Prepare and analyze clinical trial patient datasets.
• Work with laboratory, vital signs, tumor response, imaging, quality-of-life, questionnaire, and adverse event data.
• Collaborate with researchers and multidisciplinary project teams to identify technology-based solutions.
• Develop customized code using existing tools and applications.
• Validate outputs for clinical bioinformatics and technical applications.
• Act as programming lead for studies of simple to moderate complexity where assigned.
• Follow departmental SOPs and working practice documents.
• Contribute to training materials and best-practice documentation.
• Continuously develop knowledge of programming, clinical trials, technology, and the pharmaceutical industry.

Qualification & Experience

MS/MA in Computer Science, Statistics, Biostatistics, Mathematics or related field with at least 3.5 years of relevant SAS programming experience OR Bachelor’s degree in a related field with at least 4 years of relevant SAS programming experience.

Hands-on SAS programming experience is mandatory, preferably within clinical trials, pharmaceuticals, biotechnology, clinical research, or a related environment.

Skills Required

Candidates should have a solid understanding of programming languages, relational database structures, and complex data systems. Good problem-solving ability, attention to detail, organizational skills, English communication, and the ability to manage multiple assignments under demanding timelines are important for this position.

2. Feasibility Site Specialist – Remote India

Job Requisition ID: R-01363889
Employment: Full-Time
Work Mode: Fully Remote
Location: Remote, India
Schedule: Monday–Friday
Experience: 0–2 years

The Feasibility Site Specialist (FSS) serves as an important point of contact between Thermo Fisher Scientific and potential investigative sites participating in clinical research.

The specialist develops relationships with investigators and site personnel, conducts feasibility assessments, supports site identification, reviews feasibility documentation, and helps ensure that suitable investigative sites are recommended for clinical studies.

Key Responsibilities

• Gather feasibility information and contribute to local investigative site list vetting.
• Conduct pre-award site outreach using approved internal tools and external sources.
• Review Confidential Disclosure Agreements (CDAs) and feasibility survey information.
• Follow up with investigative sites regarding missing or inconsistent information.
• Coordinate feasibility site documentation collection and tracking.
• Maintain accurate site and database contact information.
• Document communication attempts with investigative sites.
• Conduct phone interviews with physicians or other site personnel where required.
• Discuss standards of care and collect protocol-level information.
• Conduct onsite feasibility visits where applicable.
• Support client calls and study-specific feasibility requirements.
• Participate in regional and country team meetings.
• Support onboarding of new employees.
• Contribute to electronic feasibility and survey tool development/testing.
• Support implementation of new departmental processes.
• Identify and escalate feasibility or system-related risks.
• Build collaborative relationships with investigative sites and site networks.
• Develop local intelligence regarding site capabilities, capacity, and expertise.
• Collaborate with Country Heads, Startup Managers, Feasibility Managers, and other study stakeholders.
• Maintain compliance with applicable systems, procedures, training requirements, and performance objectives.

Qualification & Experience

Bachelor’s degree or equivalent relevant academic/vocational qualification with 0–2 years of relevant feasibility or clinical research experience; previous CRA or other site-facing clinical research experience is preferred.

Thermo Fisher Scientific may also consider an appropriate combination of education, training, and directly related professional experience.

Can Freshers Apply?

The official requirement states 0–2 years of previous feasibility and clinical research experience. Therefore, candidates at an early-career level may be considered, but applicants should ideally have relevant clinical research exposure through employment, internships, site experience, academic projects, or comparable training.

Previous experience as a Clinical Research Associate (CRA) or in another site-facing position is preferred rather than explicitly mandatory.

Skills Required

Candidates should possess effective written and verbal communication skills, knowledge of medical terminology, interpersonal and negotiation skills, attention to documentation quality, and basic organizational and planning abilities.

Knowledge of Good Clinical Practice (GCP) and applicable SOPs is important. Candidates should also be comfortable with Microsoft Office and capable of learning clinical research software and systems.

The position may require approximately 0–20% travel, depending on business and study requirements.

Why Join Thermo Fisher Scientific?

Thermo Fisher Scientific provides opportunities to work within a large global organization supporting scientific research, healthcare, and clinical drug development.

Selected candidates may gain exposure to:

• Global clinical research projects and study teams
• Pharmaceutical and biotechnology development programs
• Clinical trial data and technology
• Cross-functional and international teams
• Structured processes, SOPs, and quality standards
• Professional learning and career development opportunities

The Feasibility Site Specialist position additionally offers a fully remote work arrangement within India, while the Programmer Analyst II position provides a hybrid working model in Bangalore.

How to Apply for

Application Link For Programmer Analyst II – Hybrid/Mid Shift

Application Link For Feasibility Site Specialist – Remote India