APCER Life Sciences India Ltd Hiring Pharmacovigilance
Associate A graduate/post graduate degree in Pharmaceutical sciences/Life
Sciences Apply Now
Job Description
Rewarding career opportunity with one of the fastest
growing organization, APCER Life Sciences.
Job Description:
Data Entry of ICSRs in APCER (ArisG, Argus
etc.)/client's pharmacovigilance database duplicate check, entering source data
in the database, MedDRA coding, narrative(s) writing, labelling of events,
report scheduling (if applicable) & attachment of source document in
database
Screening, evaluation and review of literature
articles for identification of valid/potential ICSRs for processing
Receipt and evaluation of safety data exchange
agreements (If applicable) for sharing and other obligations
Execution of organization's standard operating
procedures
Management of compliance with the organization's
standard operating procedures and regulatory requirements
Liaise effectively and maintain excellent relationship
with the internal contacts
Maintain awareness of changes to/new regulations
affecting pharmacovigilance activities
Communicate new or changed regulations to relevant
members of the department in order to initiate any change in processes
Builds and maintains good relationships across
functional units and company affiliates
Escalate critical calls to concerned managers/clients
Remain up-to-date with the latest information on the assigned product(s)
To carry out necessary administrative duties required
for the job
Other duties as assigned by management
Trains and mentors new employees in PVG (if required)
Generation and review of SOPs and WIs (if required)
Complies with applicable ISMS related procedures &
policies
Key Competencies:
Self motivated
Good competence with therapeutic and medical
terminology
Meticulous attention to detail client focused approach
Ability to follow instruction and deliver assigned
tasks within agreed timelines
Aptitude to learn new skills and enhance pharmacovigilance
knowledge
Key Skills:
Knowledge of European and ROW (if applicable)
regulatory requirements
Good time and management skills
Strong interpersonal & communication skills
Basic knowledge of Microsoft Office/Applicable
software
Qualification :
A graduate/post graduate degree in Pharmaceutical
sciences/Life Sciences
Submit your CV today to be considered for role within
our organization.
Industry : Pharma / Biotech / Clinical Research
Functional Area : Medical, Healthcare, R&D,
Pharmaceuticals, Biotechnology
Role : Documentation/Medical Writing
Keyskills : ICSR, Individual case study report, Argus,
Arisg, Data Entry, MedDRA, Pharmacovigilance, drug safety, Literature,
Duplicate search, Triage
APPLY CLICK HERE
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