Clinical Scientist Late Stage Oncology - Manager (Clinical Data Review)

The Late-Stage Clinical Scientist (non-MD, Manager) will have an emphasis on performing clinical data review in support of scientific oversight, data integrity and quality of clinical trial(s) for programs within the Late-Stage Oncology portfolio. 

ROLE RESPONSIBILITIES

• Responsible for performing clinical data review in support of scientific oversight, data integrity and quality of the clinical trial(s).
• Clinical development professional maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
• Support other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program.
• Contributes and support other clinical and medical colleagues, as appropriate.
• Reviews and queries safety and efficacy data in support of the clinical data review strategy and collection of quality data and review of emerging clinical data and trends.
• In close partnership with medically qualified colleague/s, analyzes the emerging safety profile of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they occur in the assigned trial(s).
• Follows relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures.

 

 QUALIFICATIONS

BASIC:

• Science degree (PhD, PharmD or equivalent) and minimum of 1-year Clinical Research experience in industry/CRO, or BA/BS and minimum of 5-year Clinical Research experience in a similar role in industry/CRO.
• Clinical Research experience in oncology preferred (fellowship or academia acceptable).
• Knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations.
• Demonstrates a passion for helping patients with cancer and for the science of oncology.
• Experience in performing clinical data review.
• Proven analytical skills with the ability to work on large data sets.
• Effective communication, presentation, and organizational skills to ensure coordinated and timely delivery.
• Demonstrated scientific writing skills and excellent communication skills (written and spoken) in English; scientific productivity via publications, posters, abstracts and/or presentations.

PREFERRED:

• Has a global perspective and mindset works well in a diverse team environment with colleagues from diverse cultures, backgrounds, and geographies. both as a leader and a key contributor; works effectively with internal and external partners and investigators/medical professionals 
• Proficient with basic IT; efficiently using a computer and telecommunications (voice and video) 
• Has the flexibility to adapt and navigate through an ever-changing work environment while maintaining integrity and quality in the work assigned.
• Must have the relevant personality features and competencies supporting the responsibilities:
• Demonstrates effective problem-solving, and agile decision-making in execution of Clinical responsibilities.
• Leverages knowledge and support from others related to overall objectives, strategy, critical issues, and policies.
• Embraces evolving technologies and adopts best practices aimed at improving the efficiency and quality of clinical development.
• Promotes team health and exemplifies Pfizer’s leadership behaviors and actionable attitudes. 
• Has foresight and judgment in complex decisions:
• Leverages a variety of communication tools and techniques to communicate results.
• Builds partnerships across the company to achieve the needs of the program.
• Collaborative problem solving (handles conflict constructively)
• Promotes innovation and takes appropriate risks to challenge the status quo to enhance the efficiency of current processes.
• Ability to work proactively and independently, organize tasks, time and priorities of self and others.

 
Work Location Assignment: Must be on-site an average of 2.5 days per week.

LI-PFE

The annual base salary for this position ranges from $99,900.00 to $166,500.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

Relocation assistance may be available based on business needs and/or eligibility.

Medical

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