Clario Biostatistics Medical Writer | Clinical Research
- Clario Hiring Biostatistics Medical Writer in Bangalore | Clinical Research Jobs
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Preferred Technical Skills
- Eligibility / Qualifications
- Educational Qualification
- Experience Required
- Essential Skills
- Location & Salary
- Job Location
- Application Process
- Frequently Asked Questions (FAQs)
- 1. What is the role offered by Clario?
- 2. What qualifications are eligible for this medical writing job?
- 3. How much experience is required for this role?
- 4. Is prior clinical trial experience required?
- 5. What skills are important for this role?
- 6. Does Clario provide hybrid work opportunities?
- Summary Table
Clario Hiring Biostatistics Medical Writer in Bangalore | Clinical Research Jobs
Clinical research professionals looking for medical writing and biostatistics jobs in India now have an exciting opportunity with Clario, a part of Thermo Fisher Scientific. The company is hiring experienced candidates for the role of Biostatistics Medical Writer in Bangalore. This full-time opportunity is ideal for professionals with expertise in clinical trial reporting, medical writing, statistical analysis plans, and regulatory documentation within CROs, pharmaceutical companies, and healthcare research organizations.
With increasing investments in clinical trials, drug development, cardiac safety monitoring, and healthcare data analytics, the demand for experienced medical writers and biostatistics professionals continues to grow across India’s pharmaceutical and life sciences industries. Clario is expanding its scientific and statistical reporting operations and actively seeking professionals capable of handling clinical safety reports, statistical documentation, protocol writing, and scientific communication.
Candidates with prior experience in clinical research, medical writing, biostatistics reporting, regulatory affairs, healthcare compliance, and pharmaceutical documentation will find this opportunity valuable for long-term career growth in the global clinical research industry.
Company Overview
Clario, a part of Thermo Fisher Scientific, is a globally recognized healthcare technology and clinical research organization specializing in endpoint data solutions, cardiac safety services, imaging, respiratory analysis, and clinical trial technologies.
The company supports pharmaceutical, biotechnology, and medical device organizations by helping accelerate clinical trials and improve patient outcomes through advanced scientific and digital healthcare solutions. Clario works with global sponsors and research organizations across therapeutic areas, delivering high-quality clinical evidence and healthcare analytics.
Clario is known for its expertise in cardiac safety, clinical data management, statistical analysis, medical writing, and regulatory support services. Employees gain exposure to international clinical trials, global regulatory standards, scientific reporting systems, and healthcare compliance frameworks.
Job Role & Responsibilities
Clario is hiring candidates for the role of Biostatistics Medical Writer to support cardiac safety and clinical trial reporting activities. The selected candidates will work closely with Statistical and Scientific teams to prepare high-quality scientific reports, statistical analysis plans, clinical documentation, and regulatory deliverables.
This medical writing and biostatistics role requires strong understanding of clinical trial reporting, healthcare data interpretation, scientific communication, and pharmaceutical regulations.
Key Responsibilities
- Create, edit, proofread, and finalize Expert Cardiac Safety Reports
- Prepare and review Statistical Analysis Plans in coordination with Statistical teams
- Manage project timelines during the scientific reporting phase
- Interpret information from study protocols, investigator brochures, scope of work documents, and study plans
- Write background sections using knowledge of clinical trial design and statistical methods
- Insert statistical outputs including tables, figures, and listings into reports
- Interpret statistical results and prepare clear scientific summaries
- Perform medical writing quality control checks before client submission
- Coordinate with project managers and scientific teams regarding project timelines and deliverables
- Lead medical writing activities during internal and client revision processes
- Support development of clinical trial synopsis and protocols for cardiac safety studies
- Maintain timelines for medical writing deliverables and reporting outputs
- Understand and follow FDA, EMA, ICH, and clinical trial reporting regulations
- Create document templates and maintain internal style guides based on industry standards
- Participate in cross-functional planning meetings and scientific discussions
- Contribute to manuscripts, scientific presentations, and publication writing support
- Train new team members on medical writing practices and documentation standards
- Assist in SOP creation, compliance documentation, checklists, templates, and process improvements
Preferred Technical Skills
Candidates applying for this clinical research and medical writing role should have practical knowledge in:
- Medical writing
- Biostatistics reporting
- Clinical trial documentation
- Statistical analysis plans
- Cardiac safety reporting
- Healthcare data analysis
- Regulatory compliance
- Scientific communication
- Clinical protocols
- Pharmaceutical drug development
- FDA and EMA guidelines
- ICH regulations
- Clinical research operations
- CRO documentation standards
- Statistical outputs interpretation
Candidates with prior experience in pharmaceutical research organizations, clinical trial management, healthcare consulting, regulatory affairs, and scientific publishing will have an added advantage.
Eligibility / Qualifications
Candidates interested in this Biostatistics Medical Writer vacancy should meet the following eligibility criteria.
Educational Qualification
Applicants should possess a degree in Science or Healthcare-related fields.
Eligible educational qualifications include:
B.Pharm, M.Pharm, Pharm.D, MSc, M.Sc Life Sciences, Biotechnology, Biostatistics, Clinical Research, Biomedical Sciences, Biochemistry, Microbiology, Public Health, Pharmaceutical Sciences, Nursing, Healthcare Management, Medicine, or related healthcare and life science disciplines.
Experience Required
- Minimum 4+ years of relevant industry experience
- Prior experience in medical writing or scientific writing required
- Experience in clinical trials, CROs, pharmaceutical research, or healthcare organizations preferred
- Knowledge of statistical outputs and regulatory documentation required
Essential Skills
- Strong scientific and medical writing skills
- Understanding of clinical trial regulations and reporting requirements
- Knowledge of FDA, EMA, and ICH guidelines
- Ability to interpret statistical outputs including tables and figures
- Strong verbal and written communication skills
- Good analytical and organizational abilities
- Experience with Microsoft Office, Adobe products, and Windows systems
- Ability to work independently and in collaborative project environments
- Strong time management and multitasking skills
Professionals interested in medical writing careers, clinical data management, healthcare consulting, pharmaceutical documentation, and CRO jobs are encouraged to apply.
Location & Salary
Job Location
Bangalore
Application Process
Interested and eligible candidates can apply online through the official Clario careers portal.
Frequently Asked Questions (FAQs)
1. What is the role offered by Clario?
Clario is hiring candidates for the position of Biostatistics Medical Writer in Bangalore.
2. What qualifications are eligible for this medical writing job?
Candidates with B.Pharm, M.Pharm, Pharm.D, MSc, Biotechnology, Biostatistics, Clinical Research, Biomedical Sciences, and related healthcare qualifications can apply.
3. How much experience is required for this role?
Applicants should have at least 4 years of relevant industry experience in medical writing, scientific writing, clinical research, or pharmaceutical documentation.
4. Is prior clinical trial experience required?
Yes, candidates with experience in clinical trials, CROs, pharmaceutical research organizations, or healthcare consulting are preferred.
5. What skills are important for this role?
Medical writing, statistical analysis interpretation, scientific communication, regulatory compliance, clinical trial reporting, and healthcare documentation skills are important for this position.
6. Does Clario provide hybrid work opportunities?
Yes, Clario offers a hybrid work environment along with flexible work schedules and employee development programs.
Summary Table
| Category | Details |
|---|---|
| Company | Clario |
| Department Vacancies | Biostatistics Medical Writer, Clinical Research |
| Qualification | B.Pharm, M.Pharm, Pharm.D, MSc, Biotechnology, Biostatistics, Clinical Research, Biomedical Sciences, Biochemistry, Microbiology |
| Experience | 4+ Years |
| Location | Bangalore |
To apply for this job please visit clarioclinical.wd1.myworkdayjobs.com.
