Quintiles is the only fully integrated biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. Our network of 23,000 engaged professionals in 60 countries around the globe works with an unwavering commitment to patients, safety and ethics - ensuring a higher level of healthcare for people. For our biopharmaceutical customers, we help them navigate risk and seize opportunities in an environment where change is constant.
Post : Pharmacovigilance
Job description
• To Prioritize and complete the assigned trainings on time.
• Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
• To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information; determining initial/update status of incoming events; database entry; coding AE and Products, writing narratives, Literature related activities as per internal/ project timelines.
• Ensure to meet quality and productivity standards per project requirements.
• To ensure compliance to all project related processes and activities.
• Creating, maintaining and tracking cases as applicable to the project plan.
• Identify quality problems, if any, and bring them to the attention of a senior team member.
• Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
• Perform other duties as assigned.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Good understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Standard Operating Procedures (SOPs) and work instructions applicable to the role.
• Good knowledge of medical terminology.
• Strong verbal/written communication skills.
• Good working knowledge of Microsoft Office and web-based applications.
• Strong organizational skills and time management skills.
• Ability to work as a Team Player, contribute and work towards achieving Team goals.
• Self-motivated and flexible
• Excellent attention to detail and accuracy.
• Ability to follow instructions/guidelines, utilize initiative and work independently.
• Ability to manage competing priorities and deadlines.
Candidate Profile :
PV Experienced candidates holding 2-5 years experience in core pharmacovigilance Good Attitude , Good communication skills Skill set- Case Processing
Additional Information:
Experience : 2-5 years
Qualification : B.pharm /M.pharm
Location : Bangalore
Industry Type : Pharma / Biotech / Clinical Research
Functional Area :Pharmacovigilance
Walk in date : 15th October, 2016 Time : 8:30 am,
Venue: Pride Hotel 216, E.V.R.Periyar Salai, Kilpauk Poonamallee High Road Chennai, Tamil Nadu, 600010 India
Posted By,
Rupal Shah
Quintiles
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