Instagram
youtube
Facebook

Pharmacovigilance Systems Administrator (Home-Based/Remote) Us

3-5 years
Not Disclosed
10 July 22, 2024
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About Us:

Worldwide Clinical Trials (Worldwide) is a leading global contract research organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies to advance new medications from discovery to reality. With a strong foundation in scientific expertise, our therapeutic focus spans cardiovascular, metabolic, neuroscience, oncology, and rare diseases. We develop tailored solutions to address complex challenges and expedite the path to market for our clients.

Our team of over 3,500 professionals operates across more than 60 countries, united by a common goal: to improve patient lives through innovative therapies. We are committed to fostering a diverse and inclusive environment where collaboration and creativity thrive.

Why Join Us:

At Worldwide, every team member plays a crucial role in making a meaningful difference for patients and their caregivers. Our approachable leaders, supportive teams, and inclusive culture ensure that professionals from all backgrounds can succeed and grow. We take pride in creating a workplace where people can be themselves and are motivated to excel every day.

About Our Pharmacovigilance Department:

Our Pharmacovigilance team is at the forefront of ensuring drug safety throughout the lifecycle of a compound. We monitor and review safety events globally, collaborating with clients to analyze and submit data to Investigators, Ethics Committees/IRBs, and Regulatory Agencies, driving clinical drug development forward.

Your Role:

  • System Management: Oversee the setup, management, and maintenance of Worldwide's pharmacovigilance systems to ensure compliance with SOPs, processes, and regulations.
  • Support & Troubleshooting: Handle day-to-day functions of pharmacovigilance systems, troubleshoot complex issues, and provide guidance on system use.
  • Training: Organize and conduct training sessions for staff, including onboarding related to pharmacovigilance systems.
  • Consultation: Offer expertise to PV management on complex pharmacovigilance data transfers for clients or potential clients.

What You’ll Bring:

  • Experience: 3-5 years of experience with pharmacovigilance systems.
  • Skills: Advanced understanding of pharmacovigilance systems and safety databases, along with a good grasp of medical terminology.
  • Computer Proficiency: Strong knowledge of MS Office applications (Excel, PowerPoint, Word) and relational database systems.
  • Interpersonal Skills: Positive attitude with the ability to interact diplomatically and professionally with internal and external stakeholders in a global setting.
  • Independence & Teamwork: Ability to work independently, prioritize effectively, and collaborate successfully in a matrix team environment.

Why We’re Here:

We are driven by the knowledge that our work helps improve lives. To explore more opportunities at Worldwide, visit our careers page at www.worldwide.com/careers. For additional information about us, visit www.Worldwide.com or connect with us on LinkedIn.

Equal Opportunity Employer:

Worldwide is committed to equal employment opportunities for all employees and applicants. We value diversity and strive to create an inclusive environment that supports collaboration and creativity. We provide reasonable accommodations to applicants with disabilities and welcome individuals from all backgrounds to thrive and excel in our workplace.