All roles

Drug Safety Associate Consultant

Remote · USA Full-time New today

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 tot his job Apply To this Job

Apply To This Job

Related roles

[Remote] Senior Regulatory Affairs Associate - Labeling Compliance Analytics

Remote · USA Full-time

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

Remote · USA Full-time

Regulatory Affairs Associate

Remote · USA Full-time

Clinical Data Manager 2

Remote · USA Full-time

Principal Clinical Data Manager

Remote · USA Full-time

Data Quality Lead / Data Management Lead - Oncology

Remote · USA Full-time

Manager, Clinical Data Management

Remote · USA Full-time

Program Manager, Clinical Data Science

Remote · USA Full-time

[Hiring] Manager, Clinical Data Management @Intellia Therapeutics, Inc.

Remote · USA Full-time

Senior Healthcare Data Analyst

Remote · USA Full-time

Senior Recruiter for Tech Startup

Remote · USA Full-time

Experienced Full Stack Customer Care Representative – Remote Customer Service and Support

Remote · USA Full-time

100%25 Virtual - Emergency Medicine

Remote · USA Full-time

Process Development Chemist

Remote · USA Full-time

Experienced Data Entry Clerk – Flexible Remote Work Opportunity with Competitive Hourly Rate

Remote · USA Full-time

Experienced Customer Service Associate - Temporary Role at arenaflex

Remote · USA Full-time

Senior Account Executive (Remote) – San Diego Focus

Remote · USA Full-time

Experienced Bilingual Customer Service Representative – Multilingual Support in Oak Creek, WI

Remote · USA Full-time

Remote Booking & Travel Support Specialist

Remote · USA Full-time

Benefits and Absence Representative

Remote · USA Full-time