Clarivate Pvt Ltd Walk-in Interview.Clarivate Pvt Ltd Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: Associate Pharmacovigilance Specialist/ Pharmacovigilance specialist
- Qualification: Degree in Life Sciences (Pharmacy, Pharmacology, Toxicology, Biology, Biomedical Sciences, etc.)
- Experienced: least 2 years of experience in drug safety, toxicology, pharmacovigilance
- Salary:Not Disclosed
Job Description: Greeting from Clarivate Pvt Ltd .!!!!!
Important Details :
- Location: Noida
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Title: Associate Pharmacovigilance Specialist/ Pharmacovigilance specialist
We are looking for a Life Science Content Analyst to join our team in Chennai/Noida. This is an amazing opportunity to work on OFF-X, a translational drug safety intelligence portal. The team consists of 20 people located in Spain and India and is reporting to the India-based Team Manager. We have a great skill set in the analysis of drug safety and toxicity data and we would love to speak with you if you have skills in that area
About You – experience, education, skills, and accomplishments
- Degree in Life Sciences (Pharmacy, Pharmacology, Toxicology, Biology, Biomedical Sciences, etc.)
- At least 2 years of experience in drug safety, toxicology, pharmacovigilance
- Excellent English written and oral communication skills
- Attention to detail, results orientated, enthusiastic, determined to achieve and shows commitment
It would be great if you also had . . .
- Ability to analyze large volumes of structured or unstructured data.
- Ability to delve deep into content and results.
- Interpersonal skills and the ability to work independently and collaboratively with a team
- Self-starter with the ability to multitask and prioritize across projects to meet deadlines
- Good skills of problem-solving and good judgment in decision-making and setting priorities.
What will you be doing in this role?
- Selection of appropriate scientific articles and conference content for the project.
- Analysis and interpretation of published data (clinical trials, journal articles, reviews, meta-analysis, congress communications, drug approval reports, etc.)
- Collection and curation of information on risks and safety of drug products (recording, archiving, updating and evaluating the information)
- Writing case studies, reports and reviews
- Maintain informed discussions with experts and customers
Work Mode- Hybrid
Location – Noida or Chennai
At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
