7 April, 2022
About the job
1. Drug Safety Associate with minimum 1 year Argus Experience
2. Drug Safety Associate Candidates with minimum 1 year Clinical Trial Processing Experience
3. Candidates who can speak Japanese with experience in Pharmacovigilance
Qualification – M. Pharm or B. Pharm with Diploma
• MedVigil Clinical Research was founded in 2012. We are a leading global CRO providing medical information and pharmacovigilance services to biopharmaceutical, generic pharmaceutical, consumer products, medical devices, contract research, and healthcare companies.
The ideal candidate must be a complete team player and should be focused on AE reporting and outsourced case processing in order to meet the timelines. Prior MedDRA and Argus database experience are essential.
If you fit the criteria please forward your resume to – email@example.com
I have done post graduation diploma in clinical research n Pharmacovigilance. I have basic knowledge of ICSR Case Processing, Oracle Argus ,MedDRA, WHO DD ,Special case Scenario, Clinical Research and Pharmacovigilance.
I am Dr. Harish from Telangana, India.
I have same experience in Pharmacovigilance/Drug Safety as you posted the JD.
Could you please contact me at +91-7207217261
Iam actively looking for a job in Pharmacovigilence.
I’m a fresher, actively looking for an opportunity in Pharmacovigilence.
This is pinjari Mohammed I have currently 12 months experience in pharmacovigilance. Working in Bioclinica as Drug safety associate.
Contract me 8341108653
I am working as a Drug Safety Associate in labcorp (covance) with 1 year experience .
contact me –