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Pfizer Inc. Clinical Technical Diligence Lead in Reno, Nevada

A Clinical Technical Diligence Lead is a member of the Oncology TASOT (Therapeutic Area Scientific Outreach Team), a globalteam composed of representatives from multiple functional lines who are responsible for evaluating the value of adding a clinically staged external compound or pipeline of compounds to the Pfizer Oncology portfolio.The TASOT reviews a broad landscape of all external compounds in order to identify the best compounds or pipelines to fit the Oncology Business Unit's (OBU) or Oncology Research Unit's (ORU) strategic goals for bringing in new assets. The TASOT leadership team identifies and recommends opportunities which are presented to the Oncology Triad and if approved by the Triad, advance to the Business Development Committee (BDC) for approval in principal (AiP) or final management approval (FMA) to execute clinical partnerships, in-licensing or potential merger-acquisitions.

ROLE RESPONSIBILITIES

Provides Medical and Clinical Development expertise for technical and strategic evaluation of all external compounds reviewed at the TASOT Working Team meetings to select strategic opportunities to pursue

Provides technical review and evaluation of clinical data on any compound(s)/ pipelines in consideration for a deal with respect to the likelihood of the ability to achieve technical success of a clinical development plan leading to full registration of the compounds in indications with maximum commercial value

Attends key Oncology-related Scientific Conferences to identify new assets that fit the strategic goals of the ORU/OBU for in-licensing and acquisition

Attends Business Development (BD) specific meetings with external companies to hear and evaluate clinical data presentations to identify new opportunities and to update assessments on previously reviewed opportunities

Leads Clinical Development technical assessments on an in-licensing/acquisition project review team, led by BU BD Search and Evaluation Leads, from the time of confidential presentations, through data review and creation of clinical development plans.

Works closely with the Clinical Project Management and Clinical Operations Leads in GPD, Commercial and Legal to provide DB Clinical Development technical support through a deal valuations on clinical cost estimates, timing of clinical outcome related to milestones, appropriate divisions of clinical oversight and responsibilities for execution of clinical studies between the parties in co-development deals etc....

Supports Clinical Technical Group Lead with development of presentations to the TRIAD or other senior management

Validates clinical assessment assumptions with direct discussions with external Oncologists and other key opinion leaders.

BASIC QUALIFICATIONS

Postgraduate training MD or DO degree (MD and PhD are a plus) with 10+ years industry or post graduate academia experience

Medical and scientific understanding of entire drug development process with emphasis on interpretation of clinical data to determine likelihood of successful execution of the highest value clinical development plan for the opportunity or opportunities under consideration.

Demonstration of good clinical technical data analysis skills

Good interpersonal skills and effective verbal and written communication skills in relating to senior management, colleagues and associates both inside and outside the corporation.

Ability to rapidly act upon diligence data to form an initial clinical assessment even when the clinical information may be early or have gaps

Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact."

PREFERRED QUALIFICATIONS

Postgraduate training/certification/fellowship in oncology. Additional experience with direct patient care is desirable.

Experience in both strategic and tactical early and full clinical drug development including all types of regulatory filings (INDs, CTAs, NDA/BLA/MAAs) e.g. industry experience as a Global Clinical Lead (or equivalent role)

Oncology drug development experience including interpretation of oncology safety data and response data for patients with either solid tumors or hematologic malignancies. Clinical development experience in both solid and liquid tumors highly desired

Has up to date state of the art knowledge of Oncology treatment paradigms for solid and/or liquid tumors to enable rapid drafting of clinical development plans

Track record of evaluating new compounds and opportunities in the pharmaceutical industry e.g. contributing to due diligence reviews

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
No specific travel or work requirements. Able to routinely attend team meetings or external company presentations which typically occur between 9-5 pm US ET

Last Date to Apply for Job: March 28, 2021
Eligible for Employee Referral Bonus

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Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

Medical

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EEO & Employment Eligibility:

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

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