Qinecsa Solutions Hiring Drug Safety Associate in Bangalore
Qinecsa Solutions are hiring Drug Safety Associates in Bangalore, Karnataka. This is a full time on site opportunity for those looking to get into pharmacovigilance, drug safety operations and safety database quality review.
Selected candidates will work as quality check reviewers, reviewing pharmacovigilance safety database entries to ensure the data is accurate, complete and in line with the required quality standards. The role will also involve monitoring case case processing times, providing quality feedback, tracking performance metrics and working with a range of other teams.
Candidates with a working knowledge of medical terminology, pharmacovigilance guidelines, adverse event management and experience in the use of pharmacovigilance safety databases should take a look at this opportunity.
Job Details
| Company | Qinecsa Solutions |
| Job Position | Drug Safety Associate |
| Functional Area | Pharmacovigilance / Drug Safety |
| Job Location | Bangalore, Karnataka |
| Work Arrangement | On-site |
| Employment Type | Full-time |
| Experience | Not specified in the available job description |
| Qualification | Not specified in the available job description |
| Primary Responsibility | Pharmacovigilance safety database quality review |
| Application Mode | |
| Official Application | Apply through LinkedIn |
About Qinecsa Solutions
Qinecsa Solutions is in the pharmacovigilance and drug safety services space. They provide services to the pharmaceutical and life sciences industry to support the management of product safety information and the fulfilment of applicable pharmacovigilance requirements.
This Drug Safety Associate role is all about reviewing the safety database entries for quality and ensuring that they are processed in accordance with the established case processing standards.
Job Responsibilities
The Drug Safety Associate will be primarily responsible for quality checks on the pharmacovigilance safety database entries and will provide support in terms of conformance to internal and external quality requirements.
1. Pharmacovigilance Safety Database Review
Review the safety database entries to confirm data completeness, accuracy and compliance with the requisite quality standards.
2. Adverse Event Case Processing Quality
Check the pharmacovigilance case information and ensure that the management of any adverse events is in accordance with the relevant procedures and timelines.
3. Product Complaint Processing
Support quality and timeline compliance for product complaint processing and related safety activities.
4. Regulatory Submission Timelines
Ensure compliance with all internal and external timelines relating to adverse event management, product complaint handling and regulatory case submissions.
5. Quality Feedback and Performance Monitoring
Give constructive quality feedback to team members and monitor, track and maintain the quality performance measures.
6. Cross-Functional Collaboration
Work with the relevant teams to support ongoing quality improvement and maintain compliance with the pharmacovigilance processes.
Eligibility Criteria
The job ad doesn’t state the minimum qualification or exact number of years’ experience. You’ll need to check those details via the LinkedIn application or the recruitment team.
The position description features the following knowledge and capabilities:
- Basic knowledge of medical and therapeutic terminology.
- Familiarity with pharmacovigilance terminology.
- Knowledge of the regulatory and pharmacovigilance guidelines.
- Understanding of patient safety regulatory obligations.
- Hands on experience with comparable pharmacovigilance safety databases.
- Excellent attention to detail.
- Ability to work independently in accordance with documented procedures.
- Ability to meet established quality and submission deadlines.
Skills Required
Candidates need to demonstrate the following skills:
Pharmacovigilance Knowledge
- Pharmacovigilance terminology and processes.
- Adverse event management.
- Product complaint processing.
- Patient safety regulatory requirements.
- Regulatory and pharmacovigilance guidelines.
Quality Review Skills
- Safety database quality checking.
- Data completeness and accuracy review.
- Quality performance monitoring.
- Compliance with standard procedures.
- Identification of data quality issues.
Communication and Professional Skills
- Fluent in English and excellent comprehension.
- Excellent written and verbal communication.
- Strong interpersonal skills.
- Good organisational and managerial skills.
- Team working and motivation skills.
- Goal orientated and a professional approach.
Job Location and Work Arrangement
The office is based in Bangalore, Karnataka, India.
The job ad is for an on-site role. You’ll need to be happy working from the Bangalore office.
How to Apply for Qinecsa Drug Safety Associate Jobs
Interested candidates can apply via the LinkedIn recruitment listing.
- Go to the Qinecsa Drug Safety Associate job on LinkedIn.
- Review the full job description and make sure you meet the eligibility criteria.
- Select the application option on LinkedIn.
- Submit your updated CV highlighting your relevant pharmacovigilance knowledge, safety database experience, quality review experience and exposure to adverse event processing.
- Confirm that your contact details and professional experience are clearly stated.
Candidates should highlight any experience they have with pharmacovigilance safety databases and quality checking of the safety case entries.
Frequently Asked Questions
1. Is Qinecsa Solutions hiring Drug Safety Associates in Bangalore?
Yes, Qinecsa Solutions have advertised a full time, on-site Drug Safety Associate position in Bangalore.
2. What are the main responsibilities of a Drug Safety Associate?
The role is to review the pharmacovigilance safety database entries, check for completeness and accuracy of the data, monitor the quality metrics, provide feedback and support compliance with the adverse event processing and regulatory submission timelines.
3. What qualification is required?
The job description as currently stands doesn’t specify any particular qualification. Candidates should check with the actual LinkedIn ad or the recruitment team as to what is required.
4. How much experience is required?
The ad makes no mention of a minimum number of years’ experience. It does state that the candidate will have hands-on experience with similar pharmacovigilance safety databases.
5. Is this a work from home opportunity?
No, the listing is for an on-site role and candidates should be okay with working from the Bangalore office.
6. How can candidates apply?
Candidates can apply via the official LinkedIn job posting.
Qinecsa Solutions Recruitment Summary
| Company | Qinecsa Solutions |
| Position | Drug Safety Associate |
| Department | Pharmacovigilance / Drug Safety |
| Qualification | B Pharm, MPharm, Life Sciences |
| Location | Bangalore, Karnataka |
| Employment Type | Full-time |
| Work Arrangement | On-site |
| Key Responsibility | Safety database quality review |
| Key Skills | Pharmacovigilance, medical terminology, quality checking, communication |
| Application Mode | |
| Apply Link | Apply Now |
Candidates interested in drug safety and pharmacovigilance quality review can look at this Qinecsa Solutions opportunity in Bangalore and submit their applications via LinkedIn.