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Drug Safety Associate Consultant

ClinChoice · company site51w
Posted 11 months ago — may be filled

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Company site · found 25 Sep 2026
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3+ yearsDegree requiredJapanese C1+Microsoft OfficeARGUS databaseCase ProcessingPharmacovigilanceICH-GCP

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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.

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JobClinChoice · company sitePosted 51w ago

Drug Safety Associate Consultant

Posted 11 months ago — may be filled

1 · Can you apply from ?

Not open

The ad doesn’t say — see the full posting.

4 · Your working hours

Not stated

The ad doesn’t say which hours. Ask the company.

5 · Trust

Company siteFound 25 Sep 2026
No one should ask you to pay to work.
Something wrong?Report this post

They ask for

3+ yearsDegree requiredJapanese C1+Microsoft OfficeARGUS databaseCase ProcessingPharmacovigilanceICH-GCP

Full description

Shown as posted, in English

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.