Bioclinica Drug Safety Scientist Vacancy – Candidates Apply Online
Bioclinica is an integrated clinical life science solutions provider, delivering powerful insight into clinical trial development, assuring greater client success in bringing medical therapies to market for people around the world. Drug safety specialist vacancy, Pharmacy job opening 2021. Check out all the details
Job Title: Drug Safety Scientist I
Eligibility Criteria: Any Healthcare Professional (BPharm/Mpharm/Pharm D/BHMS/BAMS, etc.) with MBA is desirable.
Experience: 4-5 years of experience in Pharmacovigilance.
Additional Skills
• Strong motivational skills and abilities, promoting a team-based approach
• Strong interpersonal and communication skills, both verbal and written
• Strong organizational and leadership skills
• Goal-oriented
• Ability to maintain a professional and positive attitude
Working Conditions:
Travel: 0-50% (can be adjusted)
Lifting: 0-50 lbs. (can be adjusted)
Other: Computer work for long periods of time
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
• Train and mentor new team members as per the requirements of the project.
• Delegate tasks and responsibilities to appropriate personnel
• Identify and resolve issues and conflicts within the project team
• Act as a 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 the 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/Database and other applicable software.
• Ability to educate/ train the team members as needed.
• Maintaining Pharmacovigilance systems including global safety database
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