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Senior Manager, Medical Field

🔥 1 hour ago

🏄 California, Hawaii, +1 more states – Remote

infoinfo

💵 $178.5k - $210k / year

⏰ Full Time

🟠 Senior

👔 Manager

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Logo of Taiho Oncology, Inc.

Taiho Oncology, Inc.

201 - 500 employees

Founded 2002

💊 Pharmaceuticals

🏥 Healthcare

Pharmaceuticals • Healthcare

Taiho Oncology, Inc. is the oncology-focused subsidiary of the Taiho Pharmaceutical Group, headquartered in Princeton, New Jersey (with U. S. sites in Pleasanton, CA and multiple international Taiho affiliates). The company concentrates on researching, developing and commercializing pharmaceutical treatments for cancer, operating as part of a global pharmaceutical organization with regional offices across North America, Europe and Asia. Taiho Oncology serves patients and healthcare providers through oncology drug development and distribution within the larger Taiho Pharmaceutical corporate structure.

📋 Description

• Serve as a field-facing representative of the Medical Affairs Department • Engage in scientific data exchange and educate healthcare practitioners on Taiho products and relevant disease states • Facilitate clinical research and implement the Medical Affairs strategic plan within the assigned geographic region • Provide clinical and scientific information to healthcare professionals • Serve as a conduit for clinical, scientific, and medical information between KOLs/investigators and Medical Affairs and development groups • Establish and maintain peer relationships with KOLs and HCPs • Present clinical and scientific data on Taiho products and relevant therapeutic areas • Identify and report scientific, clinical, and research insights from KOLs and HCPs • Respond to unsolicited medical information requests • Fulfill pharmacovigilance responsibilities related to medical inquiries and drug safety information • Develop and implement a medical territory plan aligned with Medical Affairs strategy • Maintain and demonstrate expertise in hematology-oncology, relevant disease states, study methodology, GCP, clinical information, and product data • Serve as a technical/scientific subject-matter resource to commercial personnel when requested • Identify local opportunities for Real World Evidence collaboration • Support Investigator-Initiated Trials and HCP-initiated projects • Facilitate review and follow-up of submitted IITs • Assist with Taiho-sponsored trials, including site selection recommendations, clinical data presentations, site initiation/training meetings, and communication of clinical-site insights • Support collaboration with professional organizations, societies, advocacy groups, GPOs, and large networked practices • Collaborate on Medical Affairs initiatives including publications, advisory boards, medical meetings, medical education, training, and speaker development

🎯 Requirements

• Terminal degree (MD, PharmD, or PhD) in medical or health sciences is strongly preferred or equivalent • Three years of experience in a field-facing scientific role is preferred • Medical Field experience is preferred • Pharmaceutical industry experience is preferred • One or more years of oncology experience is preferred • Knowledge of oncology KOLs, HCPs, and institutions in the geography to be covered is preferred • Knowledge of clinical trials is preferred • Knowledge of treatment guidelines, clinical research processes, FDA regulations, and OIG guidelines is required • Excellent interpersonal communication and presentation skills are required • Ability to network and partner with medical thought leaders, academic institutions, large group practices, medical directors, and pharmacy directors is required • Demonstrated ability to work cross-functionally and influence and negotiate at all organizational levels • Demonstrated ability to anticipate, organize, plan, and handle multiple changing priorities • Demonstrated ability to work independently while adhering to Medical Affairs strategic direction • Demonstrated proficiency communicating upward, downward, and laterally, verbally and in writing • Demonstrated ability to analyze complex situations, identify opportunities/issues, and solve problems across functional boundaries • Commitment to teamwork and compliance with company policies, systems, and practices • Valid driver's license • Ability to read, analyze, and interpret scientific and technical information and data • Excellent English communication skills, verbal and written • Critical thinking ability • Operational proficiency with PowerPoint, Word, and Excel • Experience working with software tracking/logging systems

🏖️ Benefits

• Annual bonus/incentive compensation plans • Potential long-term incentive plan • Discretionary awards • Medical benefits • Financial benefits • 401(k) eligibility • Paid vacation • Paid sick time • Paid parental leave

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