Thermo Fisher Scientific Hiring 2026 for Coding Specialist, Site Payment Associate & Project Manager | Remote Pharma Jobs in India

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Thermo Fisher Scientific Hiring 2026 for Coding Specialist, Site Payment Associate & Project Manager Roles (Thermo Fisher Scientific Hiring 2026) Introduction Thermo Fisher Scientific has announced multiple hiring opportunities in India for freshers and experienced professionals across clinical research, medical coding, finance operations, and project management departments. The company is recruiting for Coding Specialist, Site Payment Associate II – FSP, Principal Site Payment Associate, and Project Manager I roles in Bangalore, Hyderabad, and remote India locations. These latest pharma and clinical research jobs in India are ideal for candidates from Pharmacy, Clinical Research, Life Sciences, Biotechnology, Nursing, Finance, Engineering, and Healthcare backgrounds. Professionals looking for remote pharma jobs, CRO careers, clinical data management opportunities, and healthcare project management roles should explore these openings immediately. Thermo Fisher Scientific offers exc...

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Brillex Clinical Research Hiring Archivist, Medical Writer & Medical Monitor in Ahmedabad | Clinical Research Jobs 2026

Brillex Clinical Research Hiring for Multiple Positions in Ahmedabad | Apply Now















(Brillex Clinical Research Hiring Archivist, Medical Writer & Medical Monitor in Ahmedabad)














Introduction

The clinical research and healthcare industry in India is expanding rapidly, with increasing demand for skilled professionals in clinical operations, protocol writing, medical monitoring, and clinical documentation. Brillex Clinical Research Pvt. Ltd. has announced multiple job openings in Ahmedabad for candidates looking to build careers in the CRO and clinical research industry.

The company is hiring for Archivist, Medical/Protocol Writer (Late Phase), and Medical Monitor – Clinical Trial positions. These opportunities are ideal for pharmacy, science, and medical professionals interested in clinical trial management, regulatory documentation, protocol development, pharmacology, and medical writing.

Fresh graduates with strong communication and documentation skills can also apply for selected roles. Candidates looking for clinical research jobs in Ahmedabad, medical writing careers, CRO jobs in Gujarat, or pharmacology jobs in clinical trials should explore these opportunities.


About Brillex Clinical Research Pvt. Ltd.

Brillex Clinical Research Pvt. Ltd. is a Gujarat-based Clinical Research Organization (CRO) specializing in late-phase clinical trials, protocol development, feasibility studies, clinical documentation, and healthcare research services. The company operates from Ahmedabad-Gandhinagar and supports clinical development programs across multiple therapeutic segments.

Brillex focuses on ethical clinical research practices, regulatory compliance, and scientific documentation while offering career opportunities for freshers as well as experienced professionals in the pharmaceutical and healthcare sectors.

The organization provides exposure to:

  • Clinical trial operations
  • Medical writing
  • Protocol development
  • Regulatory documentation
  • Pharmacovigilance coordination
  • Clinical monitoring activities

Company Overview

Company Name: Brillex Clinical Research Pvt. Ltd.
Industry: Clinical Research / CRO / Healthcare Research
Headquarters: Ahmedabad-Gandhinagar, Gujarat, India
Specialization: Late-Phase Clinical Trials, Medical Writing, Protocol Development, Clinical Documentation
Company Type: Clinical Research Organization (CRO)
Employee Strength: Growing Clinical Research Team


Job Overview Summary

Brillex Clinical Research is hiring professionals for multiple clinical research positions in Ahmedabad. The recruitment includes opportunities for freshers and experienced candidates across documentation management, protocol writing, and medical monitoring operations.

These openings are highly suitable for candidates looking to build careers in:

  • Clinical Research
  • Medical Writing
  • Protocol Development
  • Clinical Operations
  • Pharmacology
  • Regulatory Documentation
  • Clinical Trial Monitoring

Professionals selected for these roles will gain exposure to late-phase clinical studies, scientific documentation, clinical operations, and healthcare compliance systems.


Vacancy Details

PositionQualificationLocationExperience
ArchivistAny GraduateAhmedabadFresher
Medical/Protocol Writer (Late Phase)Any Science GraduateAhmedabad2–6 Years
Medical Monitor – Clinical TrialMD PharmacologyAhmedabad2–3 Years

Employment Type

Full-Time

Industry

Clinical Research / CRO / Pharmaceutical Industry


Job Role Explanation

Archivist Role

The Archivist will manage clinical trial documents and ensure proper organization, storage, and retrieval of essential records. This role is suitable for freshers with good communication and documentation handling abilities.

Medical/Protocol Writer Role

The Medical/Protocol Writer will prepare scientific and regulatory documents for late-phase clinical trials. Candidates will work closely with clinical research teams for protocol drafting, clinical study reports, and scientific data compilation.

Medical Monitor Role

The Medical Monitor will provide medical oversight during clinical studies, review clinical safety data, and support protocol development and feasibility assessments. Candidates with MD Pharmacology qualifications and clinical trial exposure are ideal for this role.


Key Responsibilities

Archivist Responsibilities

  • Maintain clinical trial records and documentation
  • Organize and archive study-related files
  • Ensure proper retrieval and storage of records
  • Support compliance with documentation standards
  • Coordinate with clinical teams for record management

Medical/Protocol Writer Responsibilities

  • Prepare late-phase clinical trial protocols
  • Draft scientific and medical documents
  • Develop clinical study reports
  • Support data compilation and feasibility assessments
  • Coordinate with clinical operations teams

Medical Monitor Responsibilities

  • Review medical and safety data from clinical trials
  • Provide medical oversight during studies
  • Support protocol development activities
  • Coordinate with pharmacovigilance and clinical operations teams
  • Monitor study compliance and patient safety

Eligibility Criteria

Candidates applying for Brillex CRO jobs should fulfill the following requirements:

Educational Qualification

Archivist

  • Any Graduate

Medical/Protocol Writer

  • Any Science Graduate

Medical Monitor – Clinical Trial

  • MD Pharmacology

Experience Required

  • Archivist: Fresher
  • Medical Writer: 2–6 Years
  • Medical Monitor: 2–3 Years

Additional Requirements

  • Strong communication skills
  • Scientific documentation abilities
  • Knowledge of clinical research processes
  • Understanding of GCP guidelines
  • Ability to work in collaborative research environments

Skills Required

Candidates applying for these clinical research jobs should possess:

  • Clinical documentation handling skills
  • Knowledge of GCP and regulatory guidelines
  • Scientific and medical writing abilities
  • Protocol drafting understanding
  • Communication and coordination skills
  • Clinical trial process awareness
  • Attention to detail and accuracy
  • Team collaboration abilities
  • Regulatory compliance understanding
  • Clinical operations exposure

Professionals with strong analytical and documentation skills may have better growth opportunities in the CRO industry.


Salary Estimate

Based on current clinical research and CRO industry standards in India, the expected salary range for these roles may vary depending on experience and qualifications.

Estimated Salary Range

  • Archivist: ₹2.2 LPA – ₹3.5 LPA
  • Medical/Protocol Writer: ₹4.5 LPA – ₹8.5 LPA
  • Medical Monitor: ₹8 LPA – ₹14 LPA

Salary packages may vary depending on:

  • Experience level
  • Documentation expertise
  • Clinical research exposure
  • Medical qualifications
  • Communication skills

Why Join Brillex CRO?

Brillex Clinical Research offers excellent opportunities for candidates interested in clinical operations and medical writing careers.

Benefits of Joining Brillex

  • Exposure to late-phase clinical trials
  • Career growth in the CRO industry
  • Opportunities in protocol development
  • Experience in clinical documentation systems
  • Professional learning environment
  • Suitable openings for freshers and experienced professionals
  • Ahmedabad-based healthcare research opportunities

Candidates interested in building long-term careers in clinical research and medical writing can benefit significantly from these opportunities.


Interview Details

Selection Process

The recruitment process may include:

  • Application Screening
  • HR Interview
  • Technical Assessment
  • Documentation Review
  • Final Discussion Round

Shortlisted candidates may receive communication from the HR team regarding further interview rounds.


Required Documents

Candidates should keep the following documents ready before applying:

  • Updated Resume/CV
  • Educational Certificates
  • Government ID Proof
  • Passport Size Photograph
  • Experience Certificates (if applicable)
  • Clinical Research Training Certificates
  • Salary Documents for experienced candidates

Job Location

Work Location

Ahmedabad, Gujarat, India

Candidates willing to work in clinical research and medical writing roles in Ahmedabad are encouraged to apply.


How to Apply

Interested and eligible candidates can apply through the official application link below:

Application Link:

https://docs.google.com/forms/d/e/1FAIpQLSdTvqIkjRdNFqQyTw_McEIItj7kaLOIchH8cebVN21AykG6kA/viewform

Candidates are advised to apply as early as possible since positions may close once suitable candidates are selected.


FAQs

Q1. Which positions are available at Brillex Clinical Research?

Brillex is hiring for Archivist, Medical/Protocol Writer, and Medical Monitor – Clinical Trial positions.

Q2. Can freshers apply for Brillex CRO jobs?

Yes, freshers with good communication skills can apply for the Archivist role.

Q3. What qualifications are required for the Medical Monitor role?

Candidates must possess an MD in Pharmacology with relevant clinical trial experience.

Q4. Where is the job location?

The job location is Ahmedabad, Gujarat.

Q5. What is the expected salary range?

The estimated salary may range from ₹2.2 LPA to ₹14 LPA, depending on the role and experience.

Q6. Is clinical research knowledge required?

Yes, knowledge of clinical research processes and GCP guidelines is preferred.

Q7. What skills are important for Medical Writing roles?

Scientific writing, protocol drafting, documentation handling, and communication skills are important.

Q8. How can candidates apply?

Candidates can apply through the official Google Form application link.


Final Conclusion

The latest Brillex Clinical Research job openings in Ahmedabad provide excellent opportunities for freshers and experienced professionals looking to build careers in clinical research, medical writing, and clinical operations. Candidates can gain valuable exposure to protocol development, clinical trial documentation, medical monitoring, and healthcare compliance activities.

With growing demand for skilled professionals in the CRO and pharmaceutical research industry, these opportunities can help candidates strengthen their careers in clinical development and scientific research. Candidates passionate about healthcare research, documentation, and clinical operations should consider applying for these roles.


Disclaimer

Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.


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