Scientist for Clinical Trials-Vaccines (Director)

Pfizer; Marlow; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A global biopharmaceutical company is seeking a Clinical Program Support Specialist in Marlow, England. The role involves providing crucial clinical consulting for global programs and ensuring data integrity across Phase 1-4 studies. Candidates must possess a relevant degree and significant experience in the vaccines area. This position offers a hybrid work option and requires excellent collaboration and communication skills.

Qualifications

• Advanced knowledge of Good Clinical Practices from previous employment.
• Extensive experience in the vaccines therapeutic area.
• Proven record of writing clinical protocols and study documents.

Responsibilities

• Provide clinical and scientific program support for the global clinical sciences team.
• Design, oversee and ensure data integrity of clinical studies.
• Analyze emerging safety profiles of drugs and keep teams informed.

Skills

Clinical research process knowledge

Exceptional written and oral communication

Cross-functional collaborative skills

Education

BA/BS Degree in a science or health-related discipline

Tools

MS Word

Excel

PowerPoint

Job description

POSITION SUMMARY

You will provide clinical and scientific program support for a global clinical sciences team on a program, ensuring consistency of approach and strategy and appropriate oversight of activities within a program or provide clinical and scientific support for multiple, global, Phase 1 - 4 clinical studies. You will be responsible for clinical sciences project management support on a program level and/or responsible for studies with a high degree of complexity. You will work collaboratively with clinical colleagues and you may develop clinical development plans and study strategies in support of the plans.

POSITION RESPONSIBILITIES

• Maintain current scientific and clinical knowledge in the vaccines therapeutic and disease area(s)

• Along with the Global Clinical Lead, responsible for the design, scientific oversight, data integrity and quality of the clinical studies within the assigned program.

• Author or oversee authoring of protocols, study level informed consent documents, and contribute to authoring of site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents.

• Partner with other clinical colleagues, clinical operations and other functional lines for the successful and consistent implementation and execution of the clinical studies within the assigned program.

• Set the clinical data review strategy and lead the clinical sciences team in the collection of quality data and review of emerging clinical data and trends; reviews and queries data; presents and discusses relevant data to appropriate teams, and other internal and external stakeholders.

• In close partnership with medically qualified colleague(s), analyze 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 studies.

• Follow relevant SOPs and regulations, comply with applicable trainings, seek opportunities to further improve quality and efficiency of clinical procedures; lead or actively participate in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure.

• May supervise, mentor, and/or develop others.

REQUIRED QUALIFICATIONS

• BA/BS Degree in a science or health-related discipline

• Advanced knowledge of the clinical research process and Good Clinical Practices from previous employment experience.

• Extensive experience in the vaccines therapeutic area.

• Proven record of independently writing clinical protocols and study documents.

• Working knowledge of statistics, data analysis, and data interpretation.

• Process improvement experience

• Exceptional written and oral communication and cross-functional collaborative skills.

• Proficient in MS Word, Excel, and PowerPoint.

• Significant experience leading operational and/or strategic teams.

Work Location Assignment:Hybrid

Purpose

Breakthroughs that change patients' lives... At Pfizer we are apatient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self.Let’s start the conversation!

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

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