Drug Safety Associate Consultant

clinchoice· QPPV Office, Local Safety Support and Regulatory Intelligence
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📍 Brazil

About this role

Job Description

Job Title: Senior Executive / Specialist - Case Processing

Employment Type: Contract

Location: Brazil (Remote)

About ClinChoice

ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis.

Our global delivery network has expanded to centers and satellite offices in the United States, Mexico, United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally and globally.

We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision.

 Primary Responsibilities:

 

  • Experience in Intake/Triage, Data Entry, Quality Review, Case Finalization/Distribution of cases received from sources such as Spontaneous, Literature, Regulatory Authority, Solicited and Clinical trials.
  • Experience in raising follow-up queries, as necessary, with appropriate documentation in the safety database.
  • Experience in ARGUS database.
  • Experience in rare disease portfolio.
  • Must possess thorough knowledge of ICH-GCP, relevant GVP module, 21 CFR guidelines and other regulatory requirements.
  • Training and mentoring skill (ICSR, Safety database etc.).

 

Candidate Profile:

  • Bachelor’s or Master’s in Pharmacy / Life Sciences or above and in alignment with project / business team requirements.
  • Minimum of 3 to 5 years of relevant experience in identified functional domain/ business workstream.
  • Must have hands on experience with MS office applications (Outlook, Excel, Word, Power Point etc.).
  • Must be able to Write and speak Japanese.
  • Dynamic working hours.

Frequently Asked Questions

Is the salary disclosed for the Drug Safety Associate Consultant position at clinchoice?
The salary for this Drug Safety Associate Consultant role at clinchoice is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Drug Safety Associate Consultant position at clinchoice located?
This Drug Safety Associate Consultant role at clinchoice is based in Brazil. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Which team or department does the Drug Safety Associate Consultant at clinchoice belong to?
This Drug Safety Associate Consultant position is part of the QPPV Office, Local Safety Support and Regulatory Intelligence department at clinchoice. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Drug Safety Associate Consultant position at clinchoice?
Click the "Apply Now" button on this page. You will be redirected to clinchoice's official application portal hosted on greenhouse where you can submit your application directly.
When was the Drug Safety Associate Consultant job at clinchoice posted?
This Drug Safety Associate Consultant position at clinchoice was posted on Oct 3, 2025. Apply as soon as possible — early applications are often reviewed first.
Drug Safety Associate Consultant
clinchoice
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You'll be redirected to clinchoice's official application page on Greenhouse.