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PHARMA JOBS POST > Clinical Research > IQVIA Safety Associate Trainee job vacancy || Apply Now
Clinical ResearchClinical Research AssociateFRESHERSIQVIA hiringSafety Associate

IQVIA Safety Associate Trainee job vacancy || Apply Now

ADMIN
Last updated: March 14, 2024 4:22 pm
ADMIN 3 years ago
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IQVIA Safety Associate Trainee job vacancy || Apply Now

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Safety Associate Trainee(Campus)APPLY NOW

Safety Associate Trainee(Campus)

Job Type: Full-Time
Job Responsibilities:
Safety Associate Trainee

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

Qualifications:

• High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences
• An Individual with a minimum of a Bachelor’s Degree in scientific or healthcare discipline or allied life sciences graduation.
• Good knowledge of medical terminology and strong verbal/written communication skills.
• Ability to work as a Team Player, contribute and work towards achieving Team goals.
• Good working knowledge of Microsoft Office and web-based applications.
• Attention to detail and accuracy.
• Ability to follow instructions/guidelines, utilize initiative and work independently and manage competing priorities and deadlines
• Willingness and aptitude to learn new skills across Safety service lines.
• Strong time management skills.
• Ensure quality of deliverables according to the agreed terms.
• Demonstration of IQVIA core values while doing daily tasks – Extensive use of keyboard requiring repetitive motion of fingers.
• Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
• Regular sitting for extended periods of time.
• May require occasional travel.
• Flexibility to operate in shifts.

Essential Functions:

• 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.
• Assuming other workflow responsibilities for the assigned project as directed by Operations team member or Manager.
• Ensure to meet the expected productivity and quality standards
• Ability to identify quality problems, if any, and bring them to the attention of a senior team member/ mentor.
• Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes.
• 100% compliance towards all people practices and processes
• Perform other duties as assigned

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By ADMIN
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Sanyasi Pradhan, M.Pharm, is a pharma professional and entrepreneur with a strong background in the pharmaceutical industry, writing on jobs and global pharma updates
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