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Bristol Myers Squibb
Overview
The MSL develops and maintains relationships with Thought Leaders and Healthcare Providers to drive scientific exchange and enhance medical education. They identify medical needs within a specific geography and support clinical trial activities and research initiatives.
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Compensation
$166,090 - $201,262 / YEAR
Posted
9 days ago
The MSL develops and maintains relationships with Thought Leaders and Healthcare Providers to drive scientific exchange and enhance medical education. They identify medical needs within a specific geography and support clinical trial activities and investigator-sponsored research.
Develop and maintain relationships with Thought Leaders and Healthcare Providers to drive scientific exchange and enhance medical education. Support clinical trial activities, identify research opportunities, and provide medical insights to internal stakeholders to support business strategy.
Systimmune
The role is responsible for end-to-end safety case processing, including intake, triage, and regulatory submissions. It also involves maintaining the PV database, managing CAPAs, and ensuring global compliance and inspection readiness.
$85,000 - $115,000 / YEAR
11 days ago
Engage in peer-to-peer scientific dialogue with healthcare leaders to translate oncology science into patient care. Act as a clinical advisor to cross-functional partners and support clinical trial feasibility and execution.
$168,220 - $203,837 / YEAR
25 days ago
1 month ago
VENESCO, LLC
The Pharmacovigilance Physician provides medical oversight of drug safety data and supports risk management strategies. Key duties include conducting medical reviews of adverse events and contributing to regulatory safety submissions and reports.
Salary not listed
Kelonia Therapeutics
The Medical Director will support clinical development activities for oncology programs, including medical monitoring, safety review, and data analysis. They will also contribute to key clinical deliverables such as study protocols, investigator brochures, and regulatory submission documents.
$243,000 - $291,000 / YEAR
Onco360
The technician will assist in daily pharmacy workflow by reporting adverse drug reactions and product complaints. They will also ensure compliance with manufacturer pharmacovigilance programs and federal pharmacy regulations.
$22 / HOUR
The technician will assist in daily pharmacy workflow by reporting adverse drug reactions and product complaints within established timelines. They will also ensure compliance with manufacturer Pharmacovigilance programs and maintain accurate patient records.
$25 / HOUR
The Clinical Intervention Technician assists in daily pharmacy workflow by reporting adverse drug reactions and product complaints within established guidelines. They ensure compliance with manufacturer Pharmacovigilance programs and maintain accurate patient profiles and progress notes.
$21 / HOUR
The technician will assist in daily pharmacy workflow by reporting adverse drug reactions and product complaints within established timelines. They will also ensure compliance with manufacturer Pharmacovigilance programs and maintain accurate patient profiles.
The technician will assist the pharmacy team in daily workflow by reporting adverse drug reactions and managing product complaints. They are responsible for ensuring compliance with manufacturer pharmacovigilance programs and maintaining accurate patient records.
The Clinical Intervention Technician assists in daily pharmacy workflow by reporting adverse drug reactions and product complaints within 24 hours. They also ensure compliance with manufacturer Pharmacovigilance programs and state/federal pharmacy laws.
