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Director, Clinician (MD) Immuno


Milano, TX 76556
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Job Details

A career at Pfizer offers opportunity, ownership and impact.

All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

The Therapeutic Area (TA) Clinician - Oncology, MD is accountable for the medical &; scientific integrity of the study or studies and the well-being of the patients. This role serves as the protocol owner and applies technical and clinical/medical excellence to ensure the design of cost-efficient clinical trials to meet the needs of internal and external customers.

S/he is responsible for effective medical/scientific oversight of studies (in partnership with Clinical Scientists and Clinical Operations team members) and supports appropriate interpretation and communication of clinical trial data (including high quality regulatory submissions and product defense activities). The TA Clinician MD safeguards compliance with internal and external standards, proactively mitigates risk and manages emerging clinical issues.

The TA Clinician MD also supports the Global Clinical Lead in the Clinical Development strategy and supports the organization of expert panels and advisory board meetings to provide input into clinical plans, study design or data analysis. The TA Clinician will also be the primary contact with external investigators &; the internal study team for questions relating to clinical/medical aspects of the protocol.

In addition to study specific activities, the TA Clinician MD may provide product/program specific medical input for target product profile(s), due diligence activities on potential in-licensing opportunities and regulatory documents as appropriate (e.g. product labels, core data sheets, Investigator's Brochures, Development Safety Update Reports, Periodic Benefit-Risk Evaluation Reports).


Required: M.D. or equivalent medical qualification.

Preferred: Postgraduate training/certification /fellowship in a medical discipline or in drug development. Demonstrated scientific productivity (e.g. doctoral thesis, publications, research reports, etc.).


Previous experience with clinical research in oncology, including in academia, as an investigator, at a pharmaceutical company or CRO

1 year of post internship experience in medical care of patients

Proven track record of being a successful medical monitor at the study level or program level

Demonstrated knowledge of designing and delivering clinical program(s), to produce both timely and good quality data, including knowledge (and appropriate use) of innovative clinical trial principles and methodologies

Regulatory awareness - proven track record of proactive management of regulatory issues related to protocols and programs, including experience of interactions with regulatory authorities

Preferred: previous experience with NDA, BLA or MAA filings and defense activities


Proven ability to get results in a matrixed management environment

Demonstrated potential or ability to design, initiate and conduct clinical studies in industry, academic, or research clinic setting

Proven scientific writing skills, with strong inter-personal, written/verbal communication skills, including ability to evaluate, interpret and present complex data

Ability to review and understand the emerging safety and efficacy profile of the drug candidate; part of this skill is putting the profile in perspective with comparator agents

Collaborative problem solving

Creativity and/or ability to put innovative approaches into practice in clinical development

Ability to discuss investigator performance issues, coach and/or mentor clinical investigative site staff to achieve operational and recruitment goals and quality standards

Ability to place innovative approaches into action that focus on trial execution and site performance


Location: Virtual in Europe

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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