Job openings at Wipro, Unilever, Medtronic, Parexel, and Vee Healthtek. Careers in Pharmacovigilance, Clinical Research and Medical Coding for B.Pharm, M.Pharm and Life Science graduates. Apply now for walk-ins and remote roles.
The pharmaceutical and healthcare sectors are witnessing a significant surge in recruitment as we approach the end of 2025. Major global corporations including Wipro, Unilever, Medtronic, Parexel, and Vee Healthtek have announced multiple job openings across various domains such as Pharmacovigilance (PV), Clinical Data Management (CDM), Clinical Research and Medical Coding. These opportunities cater to a wide spectrum of professionals, ranging from fresh graduates with B.Pharm and M.Pharm degrees to experienced clinical research associates and certified medical coders.
1) Wipro Pharmacovigilance Walk-In Interview for Freshers
Wipro Limited, a global leader in information technology and business process services, is hosting a massive walk-in drive for its Pharmacovigilance department. This recruitment initiative is specifically designed for pharmacy graduates who are looking to kickstart their careers in drug safety and regulatory compliance.
Overview of the Wipro Pharmacovigilance Role
Pharmacovigilance is a critical function within the life sciences industry, focusing on the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. At Wipro, entry-level professionals are integrated into a high-tech environment where they contribute to global drug safety standards.
The role involves the systematic monitoring of pharmaceutical products to ensure they remain safe for public consumption. For freshers, this serves as an excellent gateway into the broader clinical research and pharmaceutical services industry.
Job Specifications and Requirements
Wipro is looking for candidates who meet the following criteria:
Experience: 0 to 1 years (Freshers are highly encouraged).
Qualification: B.Pharm or M.Pharm degree from a recognized university.
Licensing: A valid pharmacy license or registration with the Pharmacy Council is mandatory.
Location: The positions are based on-site at the Gurgaon facility.
Shift Work: Candidates must be willing to work in night shifts, as the operations support global clients across different time zones.
Core Responsibilities at Wipro
As an Associate in the Pharmacovigilance department, your daily tasks will include:
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Case Processing: Managing Individual Case Safety Reports (ICSRs) which involve documenting adverse events reported by healthcare professionals or consumers.
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Data Entry: Accurately inputting medical information into sophisticated safety databases.
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Triage and Assessment: Sorting cases based on seriousness and expectedness according to regulatory guidelines.
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Signal Detection Support: Assisting senior analysts in identifying patterns that might indicate a new safety risk associated with a medication.
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Compliance: Ensuring all reports are submitted within the strict timelines mandated by regulatory bodies like the FDA or EMA.
Walk-In Interview Details for Wipro
Date: 22nd and 23rd December 2025
Time: 11:00 AM to 1:00 PM (Reporting window)
Venue: Wipro Limited, Plot Number 480-481, Udyog Vihar, Phase III, Gurgaon, Haryana – 122016.
Contact Persons: Simran Sagar and Arpit Gaur.
Candidates are advised to bring an updated CV and a government-issued ID. It is important to note that the selection process may involve multiple rounds of technical and HR interviews, lasting the entire day.
2) Unilever Associate Global Market Vigilance (GMV) Recruitment
Unilever, a household name in consumer healthcare and fast-moving consumer goods (FMCG), is expanding its Wellbeing Collective team. They are currently hiring for the position of Associate in Global Market Vigilance (GMV) at their R&D hub in Bangalore.
The Role of Market Vigilance at Unilever
The Global Market Vigilance team is part of the Global Regulatory Affairs (GRA) department. Unlike traditional clinical pharmacovigilance, market vigilance at Unilever focuses on post-market safety surveillance of consumer healthcare products. This ensures that products already on the shelves continue to meet the highest safety standards for millions of consumers worldwide.
Qualifications and Experience Needed
Unilever is seeking individuals who possess:
Education: A Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related healthcare field.
Experience: 0 to 2 years in post-market safety or PV.
Technical Skills: Proficiency in using scientific databases and a foundational understanding of safety processes.
Language: Exceptional communication skills are required to coordinate with global teams and document complex medical data.
Detailed Job Responsibilities at Unilever
The Associate in GMV will be responsible for:
Intake and Triage: Receiving health-related complaints and documenting them as Adverse Events (AEs) using the Veeva Vault Safety system.
Duplicate Management: Performing thorough checks to ensure data integrity and avoid redundant case processing.
Escalation Protocols: Identifying serious cases that require immediate attention from senior management or regulatory authorities.
Collaboration: Working closely with Call Centers and R&D teams to gather missing information regarding reported cases.
Regulatory Submissions: Assisting in the preparation of case narratives and causality assessments.
Application Process for Unilever
Interested candidates should apply through the Unilever careers portal using the Job Requisition ID: R-1170195. The application deadline is set for December 31, 2025. Given the nature of the role, candidates must be prepared for a work schedule that includes significant overlap with US time zones.
Apply:
3) Medtronic Remote Opportunity: Associate Clinical Data Specialist
Medtronic, a pioneer in medical technology, is offering a unique opportunity for fresh graduates to join their clinical operations team as an Associate Clinical Data Specialist. This role is particularly attractive as it is a remote position based out of the Chennai region, allowing for a flexible work-from-home arrangement.
What is a Clinical Data Specialist?
A Clinical Data Specialist plays a pivotal role in medical device research. They are responsible for the integrity of data collected during clinical trials. This data is the foundation upon which new medical technologies are approved for use in hospitals and clinics.
Eligibility and Skills for Medtronic
Degree: A Baccalaureate degree (or equivalent) in Life Sciences or a related field.
Experience: 0 years (Entry-level).
Analytical Ability: Strong problem-solving skills to identify trends and resolve data discrepancies.
Knowledge: A basic understanding of clinical protocols and data collection systems is preferred.
Key Tasks and Performance Areas
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Study Design: Collaborating on the testing and implementation of clinical study databases.
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Protocol Development: Assisting in the creation of data systems that align with clinical protocols.
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Data Validation: Reviewing data for accuracy and ensuring cross-project consistency.
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Quality Planning: Developing data quality plans to mitigate risks of data loss or corruption.
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Reporting: Preparing comprehensive reports for internal validation and regulatory review.
This role offers a competitive salary and the Medtronic Incentive Plan (MIP), making it one of the most sought-after entry-level roles in the clinical data domain.
Apply online through the official Medtronic careers portal:
Job Requisition ID: R55390
4) Parexel Clinical Research Associate (CRA) Openings in Sao Paulo
For those looking for a career that involves travel and direct interaction with medical institutions, Parexel is hiring Clinical Research Associates (CRAs) for their operations in Sao Paulo, Brazil. Parexel is one of the world’s leading Clinical Research Organizations (CROs), providing a bridge between pharmaceutical companies and clinical trial sites.
The Impact of a CRA
A CRA at Parexel serves as the primary point of contact for clinical sites (hospitals and research centers). They ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements.
Candidate Requirements
Qualification: Degree in biological science, pharmacy, or nursing.
Experience: Previous experience in site management or clinical research is required.
Skills: Proficiency in Clinical Trial Management Systems (CTMS) and MS Office.
Mobility: A valid driver’s license and a willingness for extensive travel are essential.
Major Responsibilities of a Parexel CRA
Site Management: Leading the site from identification and initiation through to close-out.
Patient Recruitment: Developing strategies to ensure trials meet their enrollment targets.
Quality Assurance: Monitoring site performance and protecting the rights and well-being of trial subjects.
Data Integrity: Evaluating the accuracy of source documents and case report forms.
How to Apply
Apply online through the official Parexel careers portal.
Visit the job listing: Clinical Research Associate (Job ID: R0000035223) or Apply Here. Submit your resume highlighting relevant clinical research experience.
https://jobs.parexel.com/en/job/sao-paulo/clinical-research-associate/877/85505970256
5) Vee Healthtek Medical Coding Careers: Surgery Specialization
Vee Healthtek is currently hiring for various levels of Medical Coders, including Senior Coders and Quality Auditors (QA), specializing in Surgery Coding. These roles are available across multiple Indian cities, including Bangalore, Chennai, Hyderabad, and Trichy.
The Importance of Surgery Coding
Medical coding is the transformation of healthcare diagnosis, procedures, and medical services into universal medical alphanumeric codes. Surgery coding, particularly for “Same-Day Surgery,” is a specialized field that requires high precision to ensure accurate billing and reimbursement in the healthcare revenue cycle.
Hiring Criteria for Vee Healthtek
Experience: 1 to 6 years of experience in Same-Day Surgery coding.
Certification: CPC (Certified Professional Coder) or COC (Certified Outpatient Coder) is highly preferred.
Education: Graduation in Life Sciences, Nursing, or Pharmacy.
Technical Knowledge: Deep understanding of ICD-10 and CPT coding guidelines.
Responsibilities of the Coding Team
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Record Review: Analyzing medical records to accurately assign diagnosis and procedure codes.
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Compliance: Adhering to the strict standards set by healthcare payers and regulatory bodies.
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Quality Auditing: (For QA roles) Reviewing the work of junior coders to maintain high accuracy levels.
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Productivity: Meeting daily targets while maintaining the quality of the coded data.
How to Contact Vee Healthtek Recruitment
Prospective candidates can reach out to the recruitment team via the following contacts:
Ramesh M: 94432 38706
Sharmila F: 75500 13231
Vanitha U: 97907 98065
Richa: 95006 9466.
Apply:
