Remote Pharmaceuticals Jobs

The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA activities at the local level, supporting the Marketing Authorisation Holder (MAH) in maintaining product compliance throughout its lifecycle.

Dispensary duties in the Main Pharmacy including medication order and profile review and entry into Meditech Expanse Pharmacy module, checking responsibilities, trouble-shooting clinical & drug distribution issues, & acting as a resource for Pharmacy Technicians & Students. As staffing situations require, provide back-up coverage for staff on a variety of patient care units and departments including decentralized medication order and profile review and problem investigation, medication reconciliation and resolution and liaison responsibilities. Based at Oakville but will include remote coverage of other sites on nights, evenings & weekend shifts. Other duties as assigned.

As a Director, Clinical Pharmacology, you’ll be at the forefront of delivering hope to patients everywhere and expertise in clinical pharmacology strategy will be critical in accelerating the organization's mission to safely and effectively translate compounds into clinical development.

The Medical Science Liaison (MSL), is a field-based scientific expert that strategically supports the scientific and business objectives of a designated therapeutic area, Rheumatology, across the product life cycle. MSLs are the primary communicators of AbbVie science within a specific geography with healthcare professionals. MSLs are the field scientific experts on given disease states and treatment options within a designated therapeutic area.

Drive meaningful patient outcomes while transforming healthcare delivery. Be at the forefront of value-based care, partnering with field teams, interdisciplinary care members, and practices to optimize medication strategies that directly improve patient lives. Guide critical transitions of care and elevate quality measures, serving as the clinical expert who bridges the gap between complex pharmaceutical needs and real-world care delivery.

The Associate Director, Clinical Trials Services oversees a group of Clinical Biospecimen Operations Managers working on multiple projects/studies focused on delivery of Natera's testing pipeline for Pharma and Consortium/Academic studies where Natera tests are run as part of an externally sponsored clinical trial or a companion diagnostic program. This role provides direct management to individual contributors to ensure delivery of study objectives.

In this role, you will provide patient care by removing the barriers to medication access. You'll work with insurance companies and clinician offices facilitating medication approvals through prior authorizations. Also, you'll work with patients and funding sources to obtain financial assistance for high dollar co-pays, and provide phone support to patients by navigating pharmacy dispensing systems to adjudicate claims, refill medications and increase adherence.

Proactively grow the specialty pharmacy patient population by making outbound phone calls to eligible patients and enrolling them with Shields Partner Pharmacy. Educate patients on the services offered by the Shields Specialty Pharmacy Program. Communicate with patient over the phone and provide them the compelling reason why the Shields Partner Pharmacy program is superior to any other comprehensive pharmacy care model.