ICON has announced an opening for a Pharmacovigilance Reporting Associate (Submission) in India. The position is available in Chennai and Bangalore and can be performed through an office or home work arrangement.
The role focuses on the preparation, review and timely submission of pharmacovigilance and drug safety reports related to clinical trials and post-marketing activities. Candidates with a bachelor’s degree in life sciences, pharmacy or a related discipline and relevant pharmacovigilance experience can apply.
The position requires strong attention to detail, knowledge of safety reporting processes, regulatory requirements, cross-functional collaboration and the ability to manage multiple deliverables in a regulated environment.
ICON Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | ICON |
| Job Title | Pharmacovigilance Reporting Associate (Submission) |
| Department | Pharmacovigilance / Drug Safety |
| Job Locations | Chennai / Bangalore, India |
| Work Arrangement | Office or Home |
| Job Type | Full Time |
| Qualification | Bachelor’s Degree in Life Sciences, Pharmacy or Related Field |
| Experience | Relevant Pharmacovigilance / Drug Safety Experience |
| Travel | Approximately 10% |
| Requisition ID | JR159343 |
| Salary / CTC | Not specified |
About ICON
ICON is a global healthcare intelligence and clinical research organisation that supports the development of medicines and treatments. The company works across clinical research and related healthcare services with an emphasis on collaboration, quality and regulatory compliance.
Job Description
As a Pharmacovigilance Reporting Associate, the professional will support drug safety reporting activities for clinical trial and post-marketing programmes.
The role involves collecting and reviewing safety information, preparing reports, coordinating with different functional teams and ensuring that required safety submissions are completed accurately and within established timelines.
The position is particularly suited to professionals who have experience with pharmacovigilance reporting processes and understand the regulatory requirements associated with drug safety submissions.
Key Responsibilities
- Prepare and review pharmacovigilance safety reports.
- Support the preparation of periodic safety updates and individual case safety reports.
- Review safety information for accuracy, completeness and regulatory compliance.
- Collect adverse event information from clinical trial and post-marketing sources.
- Analyse relevant safety data for inclusion in safety reports.
- Maintain awareness of current pharmacovigilance reporting requirements.
- Follow applicable regulatory standards and industry practices.
- Work with clinical, regulatory, data management and other cross-functional teams.
- Collect required information from internal stakeholders.
- Investigate and resolve reporting-related issues.
- Coordinate safety reporting deliverables with relevant teams.
- Ensure safety reports are submitted to regulatory authorities and sponsors within required timelines.
- Manage multiple reporting activities while maintaining quality and accuracy.
Educational Qualification
Candidates should have:
- A Bachelor’s degree in Life Sciences, Pharmacy or a related field.
Experience Requirements
The vacancy requires relevant experience in:
- Pharmacovigilance
- Drug safety
- Safety reporting processes
- Regulatory requirements related to pharmacovigilance
The posting does not specify a fixed number of years of experience.
Required Skills
Candidates should demonstrate:
- Strong attention to detail.
- Good organisational skills.
- Ability to prepare and review complex safety reports.
- Understanding of pharmacovigilance reporting processes.
- Knowledge of applicable regulatory requirements.
- Strong written and verbal communication.
- Cross-functional collaboration skills.
- Ability to manage multiple priorities.
- Effective time management.
- Ability to work in a fast-paced and regulated environment.
Pharmacovigilance Reporting Activities
The position involves several important drug safety reporting activities, including periodic safety updates and individual case safety reports.
The Associate will work with safety information obtained from both clinical trials and post-marketing sources and help ensure that the relevant information is accurately incorporated into required safety reports.
Timely submission is also an important part of the role, requiring coordination with sponsors, regulatory teams and other stakeholders.
Work Location and Work Arrangement
The position is available at:
- Chennai, India
- Bangalore, India
The job listing specifies an Office or Home work arrangement.
The role may require approximately 10% travel, depending on business requirements.
Salary / CTC
ICON has not specified the salary or CTC for this position in the provided job posting. Candidates can refer to the official recruitment communication for compensation details.
Employee Benefits
ICON states that its total rewards package may include benefits such as:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes
- Medical, dental and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance and wellbeing resources
- Learning and development programmes
- Structured training and career development opportunities
Benefits may vary depending on the role and location.
Legal Work Requirement
Employment with ICON is subject to the candidate having the legal right to work in the country where the position is based.
Inclusion and Accessibility
ICON states that it is an equal opportunity employer and is committed to providing an inclusive and accessible workplace.
Candidates requiring reasonable accommodation during the recruitment process can request appropriate support through the company’s recruitment process.
How to Apply for ICON Recruitment 2026
Eligible candidates can apply online through the official ICON careers portal.
Candidates should review the complete job requirements and ensure they have the relevant pharmacovigilance or drug safety background before submitting their application.
Important Details Before Applying
- The position is Pharmacovigilance Reporting Associate (Submission).
- Locations include Chennai and Bangalore.
- The role is full time.
- Office or home work arrangements are listed.
- A bachelor’s degree in life sciences, pharmacy or a related field is required.
- Relevant pharmacovigilance or drug safety experience is required.
- The position involves clinical trial and post-marketing safety reporting.
- Approximately 10% travel may be required.
- Salary/CTC has not been disclosed.
- Candidates must have the legal right to work in the country where the role is based.
Frequently Asked Questions
1. What is the job title at ICON?
The position is Pharmacovigilance Reporting Associate (Submission).
2. Where is this ICON job available?
The position is available in Chennai and Bangalore, India.
3. Is this a full-time position?
Yes. The position is listed as Full Time.
4. Can the role be performed from home?
The job listing specifies an Office or Home work arrangement.
5. What qualification is required?
Candidates should have a Bachelor’s degree in Life Sciences, Pharmacy or a related field.
6. What experience is required?
Relevant experience in pharmacovigilance or drug safety is required. The vacancy does not specify a particular number of years.
7. What does the role involve?
The position involves preparing and reviewing safety reports, analysing adverse event information, coordinating with cross-functional teams and supporting timely safety submissions.
8. Which safety reports are mentioned?
The posting specifically mentions periodic safety updates and individual case safety reports.
9. Does the role involve clinical trials?
Yes. Safety reporting activities cover information from clinical trials as well as post-marketing sources.
10. Is travel required?
The vacancy states that approximately 10% travel may be required.
11. Is salary mentioned?
No specific salary or CTC is provided in the job posting.
12. What is the job requisition ID?
The requisition ID is JR159343.
Important Note
Job availability, eligibility requirements, work arrangements, benefits and recruitment conditions may change. Candidates should verify the latest information on the official ICON careers portal before applying. Benefits may vary by role and location. This article is based on the provided job information and is not an official recruitment notification issued by ICON.