Pharmacovigilance Specialist (Remote)

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Bachelor's degree in life sciences or related field is preferred., Experience in pharmacovigilance or drug safety is essential., Strong analytical skills for data review and signal detection., Familiarity with regulatory requirements and safety reporting timelines..

Key responsabilities:

  • Manage adverse event case reports and conduct follow-ups.
  • Notify regulatory agencies and respond to their requests.
  • Draft and manage periodic safety update reports and signal detection reports.
  • Provide training and support for global pharmacovigilance operations.

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Kaztronix LLC Human Resources, Staffing & Recruiting SME https://www.kaztronix.com/

Job description

Job Description
Summary: Provides operational support for global pharmacovigilance activities of marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data review, compilation, and analysis, including management of the integrated safety database. Primary responsibilities for the role: Management of Adverse Events including activities such as processing adverse event case reports and conducts follow-up . Notifies regulatory agencies and business partners accordingly; responds to requests from regulatory agencies . Reviews scientific literature and bibliographic sources; draft and manage periodic safety update reports. . Evaluates safety profiles; draft and manage signal detection reports; ensures document filing and archiving. . Participation in the processes of involving the collection, processing, review and distribution of adverse event information regarding development and marketed pharmaceutical products. Contributes to ensure compliance of pharmacovigilance activities including activities such as conduct case reconciliation with concerned departments, affiliates, distributors or business partners . Take part in self-inspection visits, audits, inspections and in CAPAs management, create or update pharmacovigilance procedures and working practices . Provide training to concerned persons based on the training plan and managing training documentation; archive documents according to prevailing standards . Support in the procedures of global pharmacovigilance operations such as Standard Operation Procedures (SOPs), internal business practices or working instructions. . Serves in an advisory capacity including activities such as product monographs review, draft responses to pharmacovigilance requests from regulatory agencies; participates in the drafting and implementation of pharmacovigilance contracts and agreements.


Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.

By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.

Required profile

Experience

Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Communication
  • Problem Solving

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