Sr Pharmacovigilance Associate
Company: Horizon Therapeutics
Location: Evanston
Posted on: January 19, 2023
Job Description:
Working at Horizon is more than a job - it's personal. For us,
success is measured by the numbers that matter most - the number of
lives we touch, the number we change and those we work tirelessly
to help save. We're a team of agile, out-of-the-box thinkers who
are inspired to do more because we know we're a part of something
bigger. We strive to build meaningful careers at a company whose
values we share because when we live up to our potential, we help
others live up to theirs.
Responsibilities:
- This Senior Associate, Clinical Safety Operations is expected
to provide PV leadership and expertise over an assigned group of
studies (Phases I-IV). Tasks include:
- Review the safety reporting section of protocols
- Develop and maintenance the SAE form for studies
- Develop and maintenance the Safety Management plan
- Support the eTMF safety sections
- Attend cross-functional study program meetings
- Support the Investigator meetings on topics such as the Study
SAE reporting
- Oversee PV vendors activities:
- Run Argus reports (master Line Listing, open activities,
submissions records)
- Receipt of SUSAR, SAE, AESI, process, review of SUSARs, quality
check, support unblinding process, and distribution to regulatory
authorities
- Manage ongoing training needs to PV Vendor
- Manage the SAE reconciliation process for all assigned programs
monthly ensuring discrepancies are resolved
- Collaborate with PV compliance and governance on quality events
relating to Clinical Safety Operations.
- Participate in process improvement projects
- Supports local inspection readiness in line with global PV
strategy
- Identify issues and raise them to help Horizon be inspection
ready and compliant.
- Archive documents per applicable internal standards and
operating procedures
- Support global medical review of pharmaceutical technical
complaints and medical information inquiries were applicable
- Assist in MedDRA coding of medical terms for clinical study
reports
- Support local PV relevant projects and document review
- Collaborate to monitor the Clinical Safety Operations
electronic mailbox
Qualifications and Skills Required:
- Nursing or Pharmacy degree plus 3+ years of
biotech/pharmaceutical experience in drug
safety/Pharmacovigilance
- Clinical/medical research experience in biotech/pharmaceutical
or clinical research organization
- Previous experience with adverse event reporting systems, FDA
and EU drug safety/Pharmacovigilance requirements
- Proactive demeanor
- Excellent written and oral skills
- Proficient in Microsoft Office
- Professional demeanor.
- Self-starter attitude.
- Strong interpersonal skills.
- Excellent written and verbal communication skills.
- #LI-Remote
Horizon Core Values & Competencies:
Growth
- Manages Ambiguity
- Strategic Mindset
- Demonstrates Self-awareness
- Cultivates Innovation
- Develops Talent
Accountability
- Drives Results
- Ensures Accountability
- Decision Quality
Transparency
- Courage
- Collaboration
- Instills Trust
#LI-Remote
Horizon Therapeutics plc does not discriminate on the basis of
race, color, religion, gender, sexual orientation, national origin,
age, disability, veteran status, or any other characteristic
protected by law. It is our intention that all qualified
applications are given equal opportunity and that selection
decisions be based on job-related factors. Any individual, who,
because of a disability, needs accommodation or assistance in
completing this application or at any time during the application
process, should contact the Human Resources Department.
Keywords: Horizon Therapeutics, Evanston , Sr Pharmacovigilance Associate, Other , Evanston, Illinois
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