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ClinChoice via Greenhouse

Drug Safety Associate Consultant

Brazil Level not stated
still open verified 1d ago posted 372d ago seen just now

Posted 372 days ago, which is unusual. The employer's own board was still carrying it when we last read it, just now.

Apply at job-boards.eu.greenhouse.io

This is the employer's own posting, not a copy on a job board.

What we know

Is it still open?

Confirmed still open

Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.

We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.

Check this listing's status as JSON

How old is it?

Posted 372d ago

The date the source published, not the day we noticed it (2025-10-03). Last seen at its source just now.

We have tracked this listing since 9 Oct 2026 (1 days). The employer's own board has carried it every time we have read it, most recently just now.

Is it remote?

The listing says yes

The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.

Who may apply?

Brazil

The description agrees: it names Brazil.

What the ad says
…Location: Brazil (Remote) A bout ClinChoice ClinChoice is a partner to…

Pay not stated

Similar roles pay $106k–161k/yr

Middle 50% of 329 listings that do state pay — Consulting · all levels · Americas · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.

Skills named in the ad

MentoringPartnershipsRegulatory Compliance

Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.

Carried by 1 source

The listing

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.
Apply at job-boards.eu.greenhouse.io