Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific. Remote pharmacovigilance role in Bangalore for experienced clinical research professionals in India.
If you are looking for a remote pharmacovigilance or clinical research job in India, this opportunity from Thermo Fisher Scientific could be a strong career move. The company is hiring Safety Reporting Specialists for a fully remote position based in Bangalore. This role is ideal for professionals with experience in safety reporting, pharmacovigilance, or clinical data review who want to work in a global CRO environment.
This position offers the chance to contribute to global drug development programs while working from home and collaborating with international clinical research teams. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Company Overview
Thermo Fisher Scientific is one of the world’s leading life sciences organizations, supporting pharmaceutical innovation through research, laboratory services, and clinical trial solutions. Through its clinical research portfolio, including PPD clinical services, the company partners with global pharmaceutical and biotech companies to accelerate drug development.
With a strong presence in clinical research outsourcing (CRO), Thermo Fisher plays a key role in delivering end-to-end clinical trial support, pharmacovigilance services, and regulatory solutions across multiple therapeutic areas. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Job Location & Employment Type
- Job Title: Safety Reporting Specialist
- Company: Thermo Fisher Scientific
- Location: Bangalore, Karnataka, India
- Work Mode: Fully Remote
- Employment Type: Full-Time
- Department: Clinical Research / Pharmacovigilance
- Work Schedule: Monday to Friday (Standard Schedule)
This remote opportunity allows professionals to work from home while contributing to international clinical safety programs.
Department Details
The role falls under the clinical safety and pharmacovigilance division, which is responsible for ensuring patient safety during clinical trials. The department handles adverse event reporting, regulatory compliance, and safety documentation for global clinical studies.
The Safety Reporting Specialist works closely with internal teams and external stakeholders to ensure accurate and timely reporting of safety data in accordance with international regulatory requirements. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Key Roles & Responsibilities
As a Safety Reporting Specialist, you will manage safety report preparation and submission activities across multiple clinical projects. Core responsibilities include:
- Reviewing, preparing, and submitting safety reports to regulatory authorities and stakeholders
- Ensuring compliance with global regulatory timelines and country-specific reporting requirements
- Managing large-scale safety reporting activities across multiple studies
- Supporting adherence to established safety workflows and internal SOPs
- Contributing to the development and refinement of procedural documents
- Collaborating with cross-functional teams on safety reporting tasks
- Participating in project meetings and providing safety updates
- Acting as a key point of contact for safety reporting within assigned projects
- Supporting new team members through mentoring and knowledge sharing
- Assisting with preparation of safety metrics and operational reports
- Contributing to project planning and limited financial tracking activities
- Maintaining high accuracy and data integrity in all safety documentation
This role requires strong ownership, accuracy, and the ability to handle critical clinical safety data. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Eligibility Criteria
Education
- Bachelor’s degree in life sciences, pharmacy, biotechnology, or related discipline
- Equivalent academic qualifications may also be considered
Relevant academic backgrounds in healthcare or biomedical sciences are preferred.
Experience
- Minimum 2+ years of relevant experience in:
- Pharmacovigilance
- Clinical safety reporting
- Drug safety operations
- CRO or clinical research environment
Candidates with prior experience in global safety reporting will have an advantage. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Skills Required
Applicants should possess the following key competencies:
- Strong understanding of medical terminology
- Knowledge of global pharmacovigilance regulations
- Proficiency in Microsoft Office tools
- Familiarity with safety databases and reporting systems
- Excellent time management and multitasking abilities
- High attention to detail and data accuracy
- Strong problem-solving and analytical skills
- Ability to collaborate with global teams
- Good communication and stakeholder coordination skills
- Ability to mentor junior team members
Candidates should be comfortable working in fast-paced clinical environments with strict compliance standards.
Salary & Benefits
- Compensation will be offered as per company norms
- Potential benefits may include:
- Remote working flexibility
- Exposure to global clinical trials
- Opportunities for career progression within a multinational CRO
- Learning and development support
- Structured work-life balance environment
Exact salary details are not specified in the job listing. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Selection Process
The hiring process generally includes:
- Online application submission
- Resume shortlisting
- Technical and functional interviews
- Final HR discussion and offer rollout
Candidates should prepare for pharmacovigilance-related questions and scenario-based discussions. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
How to Apply
Eligible candidates should apply through the official Thermo Fisher Scientific careers portal.
Before applying, ensure your resume highlights:
- Pharmacovigilance or safety reporting experience
- Knowledge of global safety regulations
- Exposure to CRO environments (if available)
- Tools and databases used in safety reporting
Applying early is recommended due to high demand for remote pharmacovigilance roles.
Important Dates
- Job Posting Status: Currently open
- Application Deadline: Not specified
Positions may close once suitable candidates are shortlisted.
Why Apply for This Pharma Job?
Here are some strong reasons to consider this opportunity:
- Work with a globally recognized life sciences leader
- Fully remote role offering location flexibility
- Opportunity to work on international clinical trials
- Exposure to advanced pharmacovigilance systems
- Career growth within a top-tier CRO organization
- Stable long-term career path in drug safety and clinical research
If you are aiming to build a future in pharmacovigilance or global clinical safety operations, this role offers valuable exposure and growth. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information website that shares verified pharmaceutical and healthcare job updates. We are not affiliated with Thermo Fisher Scientific or any organization mentioned in this article. Applicants are advised to verify job details from the official company website before applying. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
Final Words
Remote pharmacovigilance roles with multinational CROs are highly sought after in India. If you have relevant experience in safety reporting and want to grow in the clinical research domain, this is a great opportunity to consider. Update your resume, review your experience carefully, and apply as soon as possible to improve your chances of selection. Safety Reporting Specialist Job Remote Clinical Research Role at Thermo Fisher Scientific
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