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This position partners with cross functional stakeholders in support of the product safety profile and benefit risk throughout product lifecycle through signal detection, signal evaluation, and preparation of written and verbal summaries of signal management activities and risks to patient safety to present to senior management and regulatory authorities globally.
Proactively provides in person (or virtual as needed) education to defined accounts within their assigned geographies on a wide range of access and reimbursement topics and needs in support of aligned product(s) strategy. This role serves as the key contact and lead for access and reimbursement support-related matters and is responsible for being the local market access expert on payer policy coverage.
The role is within the External Capabilities group in Small Molecule Process R&D. Provides operational support and technical guidance for outsourced projects within Merck’s external CDMO partners to ensure the on time, high quality delivery of products and services. Some flexibility is required to work remotely with Merck’s overseas partners in another time zone during off hours.
As the Director, Medical Science Liaisons, you will report directly to the Vice President, Medical Affairs and will be responsible for building and leading the Medical Science Liaison (MSL) teams and collaborating with the therapeutic area Medical Directors to develop field medical strategy and tactics in support of Medical Affairs (MA) goals.
The Provider Relations Specialist serves as a key liaison between Capital Rx and its pharmacy network providers, managing provider relationships and maintaining contract integrity. This role involves resolving pharmacy inquiries and supporting network operations, ensuring smooth communication and operational efficiency across stakeholders. Responsibilities include managing accounts for designated pharmacy providers, handling contract routing, and communicating pertinent information to pharmacies.
The Associate Director of CMC Program Management will partner with the Vice President, Manufacturing Operations to oversee and execute on CMC commercial, lifecycle management, and preclinical activities at Vera. Responsibilities include developing and tracking project timelines, coordinating commercial supply readiness, and acting as a liaison between the CMC team and external partners. Candidates should be detail-oriented, self-directed, and able to manage workload to meet milestones.
The Senior Clinical Trial Manager (CTM) oversees the planning, execution, and completion of clinical trials to ensure they meet regulatory standards, timelines, and budget constraints. This role is pivotal in ensuring the integrity and success of clinical research studies.