Overview
Pharmacovigilance Associate Jobs in Oakville, Ontario at BioScript Solutions
Title: Pharmacovigilance Associate
Company: BioScript Solutions
Location: Oakville, Ontario
Job Details
DescriptionAt BioScript Solutions, we’re committed to simplifying access to specialty care for people with chronic health conditions and rare diseases. From our home base in Atlantic Canada, we’ve grown into a national network of 13 pharmacies, 100+ Coverdale Clinics, and comprehensive patient support programs (NavieGo) that serve thousands of people across the country. And together, with our third-party logistics and A&D Wholesale operations, we’re proud to be a Canadian leader in specialty health care.
Your future starts hereWe are looking for a meticulous individual with attention to detail to assume the position of Pharmacovigilance Associate (PV). The key functions include managing the collection, processing and reporting of Adverse Reactions (ARs) and Product Quality Complaints (PQPs) in accordance with corporate and national pharmacovigilance requirements (BioScript/NavieGo/CRC). In addition to these core functions, the ideal candidate would also assist with quality assurance related tasks such as; but not limited to audit preparation, CAPA investigations, change management and program compliance.
How You Will Make An Impact
Managing the collection, processing, and reporting of adverse events (AEs) and reconciliation
reports
Accountable for recognizing, triaging, and reporting as per the program or manufacturer
requirements
Maintaining high compliance standards regarding reporting timelines, quality of reporting, and
responding to inquiries from stakeholders
Help conduct Pharmacovigilance compliance activities
Assisting in the initiation of investigations for late AE reports.
Shift Rotation–8:00a.m.-4:00p.m., 9:00a.m.-5:00p.m., 10:00a.m.-6:00p.m. Occasional weekend work.
Other tasks as required
What You’ll Bring To Our Team
BSc and/or BA related to Health Science;
1-3 years of experience in Pharmacovigilance/Medical Information/Adverse Event Reporting/Safety Case Processing experience and/or Regulatory or QA is an asset;
Good understanding of safety regulations;
Experience in medical and/or pharmaceutical field(s), including exposure to medical terminology and/or scientific writing is an asset;
Exceptional organizational skills and strong attention to detail;
Proven analytical and proven solving skills;
Preference for an individual with CAPA investigation experience;
Versed in Change Control Management is an asset;
Proficient in conducting Program Compliance;
Above average verbal and written communication skills;
Demonstrated prioritization skills and ability to multi-task to meet tight deadlines;
Bilingual, English/French is a strong asset;
Comfortable working with computers and technology, specifically the Microsoft Office suite of products.
With one tree planted for every new hire, why not start your new job on a green foot and help us lower our carbon footprint.
Job Status:
Full Time, Permanent
Job Location:
Oakville, ON or Moncton, NB
Application Deadline:
June 21st, 2024
Our commitment to our team, our patients, and our community
As one of Canada’s Best Managed Companies, we offer a competitive total rewards package and paid time off to volunteer. From donation programs and local community engagement activities, to national charitable and environmental initiatives, our team’s passion for creating change extends from patient care to community care.
We’re proud to be an equal opportunity employer….
