Full-Time

Principal Programmer Analyst

Updated on 8/1/2026

Thermo Fisher Scientific

Thermo Fisher Scientific

10,001+ employees

Supplies laboratory instruments, reagents, diagnostics

No salary listed

Bengaluru, Karnataka, India

Hybrid

Occasional domestic and international travel may be required.

Category
Biology & Biotech (1)
Required Skills
Risk Management

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Requirements
  • Experience with Study Data Tabulation Model, Analysis Data Model, and Tables, Listings, and Figures is mandatory.
  • A Master of Science or Master of Arts degree in computer science, statistics, biostatistics, mathematics, or a related field and at least 6 years of relevant experience, or a bachelor's degree in those fields or equivalent qualifications and at least 8 years of relevant experience.
  • Strong Statistical Analysis System programming skills.
  • A strong understanding of database structures and complex data structures.
  • Excellent problem-solving and innovative skills.
  • Excellent written and verbal communication skills, including proficiency in English.
  • Ability to organize work independently and adapt to changing priorities across multiple assignments.
  • Ability to work and lead in a multidisciplinary team setting.
  • Ability to coach and mentor others through project leadership.
  • A good understanding of clinical trials, International Council for Harmonisation statistical and reporting guidelines, and Good Clinical Practice.
  • Excellent knowledge of statistical principles applied to the design and analysis of clinical trials.
  • A good understanding of requirements for submitting clinical data to regulatory authorities.
  • Excellent project management skills, including project budget creation and updates, and management of project budgets and risks.
  • Ability to interpret and contribute to company policies.
Responsibilities
  • Serve as a lead programmer or project lead on studies or drug programs of varying complexity and scale.
  • Work directly with project team leaders and client representatives to conduct team meetings, develop and maintain project timelines, assess and forecast resources, and ensure adherence to study budgets and contractual obligations.
  • Plan and develop tools and techniques that improve process efficiency, including leading solution teams.
  • Represent the department to clients on study matters, bid defenses, and submission or review of clinical data to regulatory authorities, and contribute directly to proposals and bids.
  • Serve as company project manager on projects limited to biometrics services when applicable.
  • Provide infrastructure support, represent the company at industry conferences, present or teach at department meetings, assist in establishing training materials, and contribute to department documents, policies, and process-improvement initiatives.
  • Increase personal and junior team members' knowledge and professional skills in programming technology and techniques, clinical trials, and pharmaceutical-industry developments.
  • Provide feedback to managers on employee performance for employee development, performance reviews, and training.
  • Increase company visibility by encouraging publication of articles in industry journals and presentations at conferences.
  • Contribute to department recruitment and candidate interview processes.
  • Occasionally drive to site locations and travel domestically and internationally.
Thermo Fisher Scientific

Thermo Fisher Scientific

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Thermo Fisher Scientific provides life sciences tools and services for research, healthcare, and industry. Its products include laboratory instruments, reagents, consumables, and software for activities like protein biology, PCR, sequencing, and bioprocessing. It differentiates itself with an end-to-end footprint across trusted brands and strong customer support and education, plus direct sales and promotions. Its goal is to help make the world healthier, cleaner, and safer by enabling discovery, diagnostics, and quality manufacturing across research institutions, healthcare providers, and government bodies.

Company Size

10,001+

Company Stage

IPO

Headquarters

Waltham, Massachusetts

Founded

1956

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Simplify Jobs

Simplify's Take

What believers are saying

  • FBI approval of RapidINTEL Plus enables CODIS searches in hours, accelerating suspect identification significantly.
  • The Arcturus partnership grants exclusive commercial manufacturing rights for ARCT-032 if the mRNA therapy succeeds.
  • LabLink 360 QA software automates QC workflows and provides real-time peer benchmarking for clinical labs.

What critics are saying

  • Biopharma funding contraction reduces 40% of revenue as Life Sciences Solutions order backlogs actively contract through 2026.
  • Academic demand collapse persists through 2026, crippling the $18.7B consumables segment reliant on university labs.
  • $9B Clario and $3.1B Olink deals fail to deliver organic growth synergies, leaving organic growth stuck at 2%.

What makes Thermo Fisher Scientific unique

  • Thermo Fisher integrates research tools with manufacturing and clinical services as a full-lifecycle partner.
  • Its unmatched breadth covers instruments, consumables, software, and biopharma services across the scientific workflow.
  • The company targets scientists with innovation while serving lab managers focused on budget efficiency via Fisher Scientific.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Unlimited Paid Time Off

Paid Vacation

Paid Sick Leave

Paid Holidays

Hybrid Work Options

401(k) Retirement Plan

401(k) Company Match

Employee Stock Purchase Plan

Fertility Treatment Support

Family Planning Benefits

Professional Development Budget

Conference Attendance Budget

Wellness Program

Mental Health Support

Gym Membership

Phone/Internet Stipend

Home Office Stipend

Company News

Keller, Inc.
Jul 2nd, 2026
Keller, Inc. to build for Thermo Fisher scientific/oakbrook Corporation.

Keller, Inc. to build for Thermo Fisher scientific/oakbrook Corporation. FITCHBURG, Wis. - Thermo Fisher Scientific, in partnership with Oakbrook Corporation (Property Manager), is moving forward with an addition to expand its loading dock capabilities. The project includes two new loading docks, an improved turning radius, and redesigned traffic flow to better accommodate semi-truck deliveries. The project is being delivered through a design-build partnership with Keller, Inc., an award-winning, 100% employee-owned design-build contractor headquartered in Kaukauna. Thermo Fisher Scientific selected Keller after previous conversations about the design-build process and identified this project as an ideal opportunity to implement the delivery method for the first time. Designed to enhance operational efficiency, the project includes selective demolition of an existing area inside the current loading dock footprint to create a more functional and productive space. Once complete, the improvements will support increased productivity for a growing business unit. Construction is scheduled to begin this summer, with completion anticipated in Fall 2026. More projects. CLINTONVILLE, Wis. - Hoffmaster has partnered with Keller, Inc. on an 86,000 sq. ft. addition and expansion project at its MENASHA, Wis. - Unison Credit Union is moving forward with the construction of a new 3,648 square foot facility in GREEN BAY, Wis. - BayCare Clinic Pain & Rehab is moving forward with the construction of a new 15,926-square-foot medical KAUKAUNA, Wis. - Accurate Machine Co., Inc. is moving forward with a 1,740 square foot PEMB addition at its facility

EC Assets
Jul 2nd, 2026
Arcturus Therapeutics gains 5.8% on Thermo Fisher deal.

Arcturus Therapeutics gains 5.8% on Thermo Fisher deal. July 2, 2026 at 13:01 GMT EC Assets Editorial Arcturus Therapeutics Inc. shares increased by 5.8% in premarket trading on Thursday, July 2, 2026. This gain follows the announcement of a collaboration with Thermo Fisher Scientific. Arcturus Therapeutics Holdings Inc. has entered into a manufacturing and clinical research partnership with Thermo Fisher Scientific. The collaboration focuses on advancing ARCT-032 for cystic fibrosis. Arcturus Therapeutics will receive up to $3 million from Cystic Fibrosis Foundation Therapeutics for this LUNAR-formulated mRNA CFTR therapeutic. Freedom Broker initiated coverage on Arcturus Therapeutics with a Buy rating on July 2, 2026. Twelve analysts have set an average twelve-month price target for Arcturus Therapeutics at $25.44. Arcturus Therapeutics Holdings Inc. stock currently stands at $6.8900 as of 02:00. The stock experienced a change of +2.53% from the previous day. Sources: investing.com, marketbeat.com, finance.yahoo.com, streetinsider.com, wallstreet-online.de, indeed.com, news.stocktradersdaily.com, lqventures.com, stocktitan.net, facebook.com.

CAP TODAY
Jun 26th, 2026
Thermo Fisher launches LabLink 360 QA software.

Thermo Fisher launches LabLink 360 QA software. June 26, 2026 - Thermo Fisher Scientific has launched the Thermo Scientific LabLink 360 Quality Assurance software, designed to help clinical laboratories simplify quality control workflows, accelerate QC review and decision-making, improve visibility into QC performance, and manage QC operations. The software consolidates QC data, automates routine review steps, and surfaces actionable insights through data visualizations and a centralized dashboard that brings all QC metrics into a single, actionable view. Built-in peer group benchmarking enables real-time comparison directly within daily QC workflows, while affiliated lab management provides unified oversight across multisite and referral networks. The software complements the Thermo Scientific MAS Quality Controls portfolio and integrates with MAS Max Load and Go automation workflows for high-volume and automated testing environments.

Applied Clinical Trials
Jun 18th, 2026
2026 DIA Global Annual Meeting: what drives sponsors to mixed outsourcing models and what the transition looks like.

2026 DIA Global Annual Meeting: what drives sponsors to mixed outsourcing models and what the transition looks like. In this video interview from the 2026 DIA Global Annual Meeting, Nick Scott of Biogen and Samantha Hadfield of Thermo Fisher Scientific, explain why mixed FSP models are becoming a strategic tool for sponsors seeking greater agility and how geography and portfolio structure shape the decision. Full interview summary. In a recent video interview with Applied Clinical Trials at the 2026 DIA Global Annual Meeting, Nick Scott, head of strategic resourcing and performance optimization at Biogen, and Samantha Hadfield, vice president of operational delivery at PPD FSP Solutions, Thermo Fisher Scientific, discussed the drivers and dynamics of mixed outsourcing models in clinical operations, following a session moderated by ACT Senior Editor Andy Studna. Scott opened by framing Biogen's move to a mixed FSP model as part of a broader strategic journey to accelerate drug development and allocate resources more deliberately - retaining core competencies in-house while leveraging external partners in areas where building that capability internally does not make strategic sense. Hadfield added a geographic dimension to that framing, describing how large pharma companies often use FSP FTEs to maintain dedicated presence in core countries while relying on unitized FSO arrangements to provide flexibility in markets with lower clinical activity. On the question of where mixed models create the most meaningful gains, both speakers pointed to portfolio dynamics as the primary driver. For Hadfield, the value is most evident when a sponsor's portfolio diversifies or expands - whether through organic growth or M&A - and the ability to bring in the right therapeutic expertise at the right time without growing internal infrastructure becomes a competitive advantage. Scott framed it around volume thresholds, noting that a full FSP model becomes more viable as volume grows, while the mixed approach provides a practical and efficient solution during the earlier or lower-volume phases of a sponsor's development program. The conversation closed on the importance of partnership fundamentals - communication, expectation alignment, shared accountability, and cultural understanding. Both speakers emphasized that the success of any mixed model comes down not just to the model itself but to the deliberateness of the journey: a clear vision of the end state, a well-documented implementation plan, and the kind of trust that allows both sides to solve problems together rather than deflect blame.

PUXANO
Jun 11th, 2026
PUXANO presents Tilted Graphene Grids at the Cambridge CryoEM Consortium.

PUXANO presents Tilted Graphene Grids at the Cambridge CryoEM Consortium. 11 june 2026. PUXANO attended the Cambridge CryoEM Consortium Biannual Meeting in Cambridge, UK, organized by Thermo Fisher Scientific. The meeting brings together leading cryoEM experts from academia and industry, including representatives from GSK, AstraZeneca, Nxera, UCB Pharma, Astex, the MRC Laboratory of Molecular Biology (LMB), and the University of Cambridge. Earlier this month, PUXANO attended the Cambridge CryoEM Consortium Biannual Meeting in Cambridge, UK, organized by Thermo Fisher Scientific. The meeting brings together leading cryoEM experts from academia and industry, including representatives from GSK, AstraZeneca, Nxera, UCB Pharma, Astex, the MRC Laboratory of Molecular Biology (LMB), and the University of Cambridge. PUXANO was invited to present its recent developments in sample support technologies, with a particular focus on its Tilted Graphene Grids. The invitation reflected growing interest in new approaches for tackling challenging cryoEM samples and improving data collection outcomes. During the meeting, its CEO, Wouter Van Putte, shared the latest results from its work on graphene-coated and tilted grids. These technologies are designed to help overcome common challenges in cryoEM sample preparation and data acquisition, making them particularly relevant for difficult biological specimens. The event provided an excellent opportunity to exchange ideas with researchers and industry scientists working at the forefront of structural biology. Beyond presenting its own work, Puxano greatly appreciated the high-quality talks covering the latest advances in cryoEM technologies, methodologies, and workflows. Meetings like the Cambridge CryoEM Consortium are valuable opportunities to gather feedback from experienced users, discuss emerging challenges in the field, and explore future collaborations. Puxano is grateful to the organizers, and in particular Pablo Castro Hartmann, for the invitation and for hosting such a well-structured and insightful event. Puxano look forward to continuing these discussions and further advancing cryoEM sample support technologies for the structural biology community.