← all jobs

Drug Safety Associate Consultant

Work from home Full-time role Hiring

Title Drug Safety Associate Consultant Location Brazil United States Employment Type Contract Location Brazil (Remote)

Job Description

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 To this Job

More open positions

[Remote] Senior Regulatory Affairs Associate - Labeling Compliance Analytics

Work from home Full-time role

MYRIAD GENETICS, INC. Regulatory Affairs Associate II (Remote/Hybrid) in SALT LAKE CITY, Utah

Work from home Full-time role

Regulatory Affairs Associate

Work from home Full-time role

Medical Device Regulatory Affairs Specialist

Work from home Full-time role

Clinical Data Manager 2

Work from home Full-time role

Analyst, Financial Reporting & Analysis

Work from home Full-time role

Remote Truck Dispatch Manager

Work from home Full-time role

[Remote] Machine Learning Engineer, Zillow Shopping AI

Work from home Full-time role

Experienced Remote Data Entry Representative – Flexible Part-Time or Full-Time Opportunity

Work from home Full-time role

Fractional CFO

Work from home Full-time role

Sr Program Mgr

Work from home Full-time role

CAD Drafter (AutoCAD – Commercial Drawings)

Work from home Full-time role

Remote Data Entry Specialist – Healthcare Documentation & Interoperability Support for careerzynith

Work from home Full-time role

Business Analyst (My Kyivstar)

Work from home Full-time role

Director, Analyst B2B Content Marketing (Remote - US)

Work from home Full-time role

Urgent Care Nurse Practitioner, Weekend Only

Work from home Full-time role

Remote Entry-Level Data Entry Specialist – Precise Data Management & Support Role at careerzynith

Work from home Full-time role

SOC Support Specialist- Eastern Time Zone

Work from home Full-time role

TMF Lead II (LATAM)

Work from home Full-time role

Regional Safety, Health & Environmental Manager II (Construction)

Work from home Full-time role

Remote Part-time ENGLISH Teacher (k-12 and/or ESL)

Work from home Full-time role