Back

Drug Safety Associate Consultant

Worldwide Salaried Open

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 tot his job Apply To this Job

More jobs

[Remote] Senior Regulatory Affairs Associate - Labeling Compliance Analytics

Worldwide Salaried

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

Worldwide Salaried

Sr. Clinical Data Manager

Worldwide Salaried

Senior Manager/Associate Director - Regulatory Operations

Worldwide Salaried

Regulatory Affairs Business Analyst in Cambridge, MA (or remote)

Worldwide Salaried

Sr Reg Affairs Spec

Worldwide Salaried

Manager of Clinical Documentation (CCDS Required), Partial Remote - Clinical Data Management

Worldwide Salaried

Senior Clinical Data Manager - 6084

Worldwide Salaried

Sr. Clinical Data Manager

Worldwide Salaried

Analyst I, Global Data Manager

Worldwide Salaried

Construction Accounting Manager- Remote for DFW area Applicants ONLY

Worldwide Salaried

Experienced Full Stack Software Engineer – Web & Cloud Application Development

Worldwide Salaried

Instructor or Assistant/Associate Professor

Worldwide Salaried

Experienced Part-Time Data Entry Clerk – National & Local Paid Focus Groups, Clinical Trials, and Phone Interviews

Worldwide Salaried

Experienced Customer Service Representative – Remote Opportunity at arenaflex

Worldwide Salaried

Work From Home - Financial Services Associate

Worldwide Salaried

Hospice Social Worker, PRN

Worldwide Salaried

Experienced Customer Support Team Leader – Remote Opportunity to Shape arenaflex's Global Support Operations

Worldwide Salaried

Customer Service Professional – Remote Servicemembers Group Life Insurance Support Specialist at arenaflex

Worldwide Salaried

Experienced Remote Data Entry Assistant – Entry-Level Opportunity with arenaflex

Worldwide Salaried