Clarivate Hiring for Associate Pharmacovigilance Specialist in Noida for literature screening, case evaluation, safety data extraction, and drug safety compliance.
Clarivate, a global leader in data analytics, scientific intelligence, and healthcare insights, is inviting applications for the position of Associate Pharmacovigilance Specialist. This role focuses on literature screening, adverse event identification, safety data management, and supporting pharmacovigilance operations. The position is based in Noida with a hybrid work arrangement, making it ideal for candidates seeking both flexibility and a strong career path in drug safety. Clarivate Hiring for Associate Pharmacovigilance Specialist
This comprehensive job post explains the responsibilities, required qualifications, industry relevance, and the complete application process. If you have at least one year of experience in pharmacovigilance, clinical research, or life sciences data review, this is an excellent opportunity to join a respected organization known for its commitment to innovation and global drug safety standards. Clarivate Hiring for Associate Pharmacovigilance Specialist
About Clarivate and Its Pharmacovigilance Function
Clarivate supports pharmaceutical companies, regulatory authorities, research organizations, and healthcare firms with world-class scientific and clinical information. Their pharmacovigilance division works with advanced data systems and structured workflows to ensure that drug safety information is monitored, identified, and escalated according to worldwide regulatory guidelines. Clarivate Hiring for Associate Pharmacovigilance Specialist
The Associate Pharmacovigilance Specialist role contributes to the company’s mission by ensuring that literature-based safety data is accurately reviewed and documented. As literature screening plays a major role in identifying early safety signals, this position is crucial for safeguarding public health and supporting regulatory compliance. Clarivate Hiring for Associate Pharmacovigilance Specialist
Position Overview: Associate Pharmacovigilance Specialist
- Job Title: Associate Pharmacovigilance Specialist
- Work Type: Hybrid
- Location: Noida
- Job Requisition ID: JREQ134249
- Employment Type: Full-time
The role involves systematic screening of scientific publications, journal articles, case reports, and medical literature to identify potential adverse events or emerging safety concerns. Under supervision, the specialist is responsible for extracting relevant data, documenting findings, and ensuring that potential cases are escalated for further processing. Clarivate Hiring for Associate Pharmacovigilance Specialist
This job is ideal for candidates with scientific backgrounds who want to build expertise in pharmacovigilance, drug safety, and literature-based signal detection. Clarivate Hiring for Associate Pharmacovigilance Specialist
Detailed Job Responsibilities
The job responsibilities have been expanded into a long-format, SEO-optimized explanation to fit into a high-quality job posting. Clarivate Hiring for Associate Pharmacovigilance Specialist
1. Literature Evaluation and Case Identification
One of the core responsibilities is to evaluate medical and scientific literature to identify:
- Potential adverse drug reactions
- Serious and non-serious adverse events
- Emerging safety concerns
- New safety signals
- Case reports requiring follow-up
The specialist must thoroughly assess articles published in medical journals, clinical research publications, and drug safety databases. Under supervision, the candidate must determine whether an article contains valid safety-related information and escalate it for further evaluation when necessary. Clarivate Hiring for Associate Pharmacovigilance Specialist
2. Extraction of Safety Data
The Associate Pharmacovigilance Specialist is expected to extract all important safety-related elements from identified literature sources, such as: Clarivate Hiring for Associate Pharmacovigilance Specialist
- Drug name and product details
- Patient information (when available)
- Adverse events reported
- Severity and seriousness of the event
- Reporting source
- Study or case details
- Any additional contextual data
Ensuring accuracy and completeness is crucial because the extracted information becomes part of regulatory submissions and internal safety reviews. A high level of attention to detail is essential. Clarivate Hiring for Associate Pharmacovigilance Specialist
3. Data Entry and Documentation
Once relevant safety information is extracted, the next step is:
- Entering validated data into pharmacovigilance platforms
- Maintaining accurate records of literature screening activities
- Documenting screening results for internal audits
- Updating tracking systems
- Ensuring all documentation aligns with company and regulatory standards
Proper documentation ensures transparency during audits and helps in maintaining the integrity of the safety monitoring process. Clarivate Hiring for Associate Pharmacovigilance Specialist
4. Regulatory Knowledge and Best Practices
Drug safety regulations continue to evolve. Candidates in this role must:
- Stay updated on global pharmacovigilance guidelines
- Understand safety reporting timelines
- Learn literature monitoring requirements for various markets
- Follow Good Pharmacovigilance Practices (GVP)
- Apply updated knowledge to daily screening activities
Regulatory awareness is essential to maintaining compliance with agencies such as EMA, FDA, MHRA, and other global authorities. Clarivate Hiring for Associate Pharmacovigilance Specialist
5. Support in Pharmacovigilance Signal Detection
The role supports early identification of safety signals. Through systematic literature review, the specialist helps detect:
- Patterns or clusters of adverse events
- New or unexpected reactions
- Worsening trends in safety data
- Safety concerns requiring immediate attention
This is a critical process in ensuring long-term patient safety and product monitoring.
Minimum Qualifications
Candidates applying for this position must have the following qualifications:
Educational Requirements
A Bachelor’s degree or equivalent in:
- Pharmacy
- Life Sciences
- Nursing
- Biotechnology
- Biochemistry
- Microbiology
- Or any related scientific field
This ensures that candidates understand fundamental biomedical concepts, anatomy, physiology, drug mechanisms, and clinical research principles. Clarivate Hiring for Associate Pharmacovigilance Specialist
Professional Experience
- Minimum 1 year of relevant experience in pharmacovigilance, drug safety, medical writing, literature screening, clinical data review, or related field.
Hands-on experience ensures that the candidate can understand medical terminology, safety reporting workflows, and scientific publications. Clarivate Hiring for Associate Pharmacovigilance Specialist
Job Category Summary: Importance of Literature Screening in Pharmacovigilance
Pharmacovigilance literature screening is a critical activity where professionals systematically evaluate scientific publications to detect potential adverse drug reactions. The process ensures: Clarivate Hiring for Associate Pharmacovigilance Specialist
- Compliance with global safety regulations
- Early identification of new safety signals
- Accurate and timely adverse event reporting
- Enhanced drug safety monitoring
Professionals in this domain must critically review journal articles, clinical study results, case reports, and peer-reviewed scientific documents. The goal is to identify any drug-related risk that requires further evaluation or reporting to regulatory authorities.
The Associate Pharmacovigilance Specialist role provides exposure to international drug safety processes and helps build strong analytical and scientific skills. Clarivate Hiring for Associate Pharmacovigilance Specialist
Equal Opportunity Statement
Clarivate provides equal employment opportunities without discrimination based on gender, race, religion, nationality, disability, age, or any other status protected by applicable laws. The company adheres to all employment regulations across jurisdictions in which it operates. Clarivate Hiring for Associate Pharmacovigilance Specialist
How to Apply for Associate Pharmacovigilance Specialist at Clarivate
Eligible candidates can apply by following the steps:
- Prepare an updated resume highlighting your pharmacovigilance experience, literature evaluation skills, and academic background.
- Visit the official Clarivate Careers Portal.
- Search for the requisition ID: JREQ134249.
- Click on the job title “Associate Pharmacovigilance Specialist” under Noida location.
- Review the job description and complete the online application.
- Upload your resume and necessary documents.
- Submit the application and monitor your email for further communication from the HR team.
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