Bioclinica Hiring Any Healthcare Professional (B.Pharm, M.Pharm, Pharm D) for Drug Safety Scientist Apply Now
Bioclinica Recruitment 2021.Bioclinica Notification full detailes below.Bioclinica is specifically structured to create clarity in the clinical trial process—so you can make better decisions. Bioclinica is divided into three business segments to deliver focused service supporting multifaceted technologies.
Important Vacancy details:
A. Post Name: Drug Safety Scientist I
B. Education: Any Healthcare Professional (BPharm/Mpharm/Pharm D/BHMS/BAMS, etc.) with MBA is desirable.
C. Experience: 4-5 years of experience in Pharmacovigilance.
D. Location:Mysore, India
Job Description: Hiring For Drug Safety Scientist I in Bioclinica !
PRIMARY RESPONSIBILITIES
As a Drug Safety Scientist, I:
• Review and evaluate AE case information to determine required action based on and following internal policies and procedures.
• Process current incoming cases in order to meet timelines.
• Provide guidance for Data entry & Quality teams.
• Following up with sites regarding outstanding queries.
• Follow-up on reconciliation discrepancies.
• Follow departmental AE workflow procedures.
• Train and mentor new team members as per requirements of the project.
• Delegate tasks and responsibilities to appropriate personnel
• Identify and resolve issues and conflicts within the project team
• Act as guide, coach and counselor for the team
• Following up with sites regarding outstanding queries and reconciliation of discrepancies
• Closure and deletion of cases
• Follow departmental AE workflow procedures
• Oversee, mentor and guide the activities of the Drug Safety and Senior Drug Safety Associates
• High level of proficiency at all workflow tasks
• Perform any other drug safety related activities as assigned.
SECONDARY RESPONSIBILITIES
• Subject Matter Expertise in Safety database
• Must have good presentation skills and the ability to give presentations.
• Knowledge of the Life Sciences Industry a plus.
• Experience in entire drug development life cycle.
• Relevant product and industry knowledge
• Experience with relevant safety databases and software applications.
• Person should be familiar with MS Office tools/Data base and other applicable software.
• Ability to educate/ train the team members as needed.
• Maintaining Pharmacovigilance systems including global safety database
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