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    • Professionals in this field protect public health by monitoring drug safety across clinical trials and post-market use.
    • Pay: Up to ₹340,000.00 per year.
    • The main goal of this role is to maintain and manage the strong relationship with clients, communicate regularly with client and update about ongoing services…
    • Study.com is the leading educational website with lessons, courses and practice for students, teachers, and adult learners.
    • All work is paid per piece.
    • Employment Type:* Full Time, Permanent.
    • We are seeking a detail-oriented Clinical Data Management Executive to manage, review, and maintain clinical trial data…
    • The Clinical Data Management Associate will assist in managing clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements…
    • Clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all.
    • 1+ yr of experience in Drug Safety and.
    • Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post-marketing surveillance.
    • Ensure compliance with regulatory guidelines for drug…
    • Responsible for performing the weekly review of literature articles for signal detection and identification of safety reports.
    • For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and…
    • This is an excellent opportunity for freshers who want to start their career in the pharmacovigilance and drug safety field.
    • Conceptualise and conduct clear, logical and compelling research studies that highlight the challenges relating to children and collect evidence for solution.
    • Junior Data Analyst (1 to 4 years experience into PV) Responsibilities.
    • Triage & intake of ICSRs in ARGUS databases within agreed timelines.
    • Acquiring comprehensive knowledge of the product portfolio and safety profiles for products across therapeutic areas.
    • Line management for assigned personnel.
    • Scientific function responsible to support a global pharmacovigilance system (both development and post marketing).
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    • Support database testing: Help validate study databases before activation.
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Job Post Details

Pharmacovigilance - job post

KLINSCIENCE HEALTHCARE
Pune, Maharashtra
Up to ₹3,40,000 a year

Job details

Pay

  • Up to ₹3,40,000 a year

Job type

  • Student job
  • Fresher
  • Full-time

Location

Pune, Maharashtra

Benefits

Pulled from the full job description

  • Paid sick time
  • Provident Fund
  • Flexible schedule

Full job description

Pharmacovigilance involves collecting, detecting, assessing, and preventing adverse effects from pharmaceutical products. Professionals in this field protect public health by monitoring drug safety across clinical trials and post-market use

Core Responsibilities Daily duties in drug safety revolve around tracking, analyzing, and documenting patient responses to medication: [1, 2]

  • Adverse Event Processing: Recording and analyzing Individual Case Safety Reports (ICSRs) detailing adverse drug reactions (ADRs).
  • Safety Data Entry: Inputting safety data into global databases (e.g., Oracle Argus) and standardizing medical terminology.

Pay: Up to ₹340,000.00 per year

Benefits:

  • Flexible schedule
  • Paid sick time
  • Provident Fund

Work Location: In person

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