Senior Epidemiologist

3 weeks ago


London, United Kingdom Thermo Fisher Scientific Full time

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global contract research organization (CRO).

The Epidemiology & Scientific Affairs (ESA) team within PPD combines epidemiology, outcomes research, biostatistics and statistical programming, and in order to support our clients in the pharmaceutical/ biotechnology/ medical device industries in building real-world evidence to demonstrate and support the clinical, economic and humanistic value of their products. We understand our clients’ needs, and we support the design and conduct of real-world observational studies throughout the product development and lifecycle, from early pre-launch planning to launch and post-marketing management. Our passionate team works hard to address real-world research questions to help fill in the gaps of burden of disease and unmet needs, describe treatment patterns, drug utilization, and adherence, understand resource utilization and costs of care, identify risk factors on disease outcomes, and outline post-marketing effectiveness and safety through post-authorization safety studies and comparative effectiveness studies. We conceptualize sophisticated study designs and develop/oversee study documents such protocols, case report forms, statistical analysis plans, analysis interpretation and study reports.

Join our growing team of dedicated scientists where you will get to work on complex, engaging projects. Our focus is on advising our clients on their real-world evidence development plans, on de novo (field, primary) data collection studies such as single and multi-country retrospective chart reviews, surveys, prospective studies and registries, which are undertaken when existing healthcare databases cannot be used. Increasingly, hybrid studies that invoke the use of both secondary data sources with tailored data collection methods are deployed. We are constantly working on new and innovate solutions to address our clients’ needs. You would be joining a team of recognized industry guides who provide top methodological expertise and high levels of quality in a collaborative environment conducive to career growth. Whether you are looking to expand your knowledge and scientific skills or step into a leadership position, we are looking for a self-motivated, driven standout colleague who will thrive in this environment.

Position Location: North America or EMEA, office-based or 100% remote.

Position Overview:
The Senior Epidemiologist leads the organization and management of research projects under the direction of senior staff. Day-to-day tasks include: drafts project deliverables and other study documents, interacts with clients and internal project team members, and contributes to critical thinking under the direction of senior staff. Supports scientific coordination and project management, including scoping, tracking progress, and coordinating team tasks for multiple projects.

Essential Duties and Responsibilities (other duties may be assigned):
The Senior Epidemiologist will lead and provide oversight on the design and implementation of de novo data collection studies (retrospective, prospective, and/or cross-sectional) under oversight of more senior staff.

In particular, you will:

- Provide scientific guidance/consultation on methodological and operational considerations of study design and conduct
- Lead or oversee the development of draft scientific project deliverables (e.g., protocols, case report forms (electronic or paper), statistical analysis plans,, reports) for senior review.
- Draft project deliverables (e.g., protocols, analysis plans, reports,) for senior review, and draft abstracts and manuscripts as lead or co-author.
- Directly contact study sponsors, physician guides, and clinical sites
- Assist the responsible scientist with monitoring project budget spend and managing timelines for scientific tasks/deliverables.
- Lead client-facing meeting and represents the project team.
- In some client engagements, serve as Principal Investigator, with final responsibilities for project budget, deliverables and timelines
- Contribute to the growth of PPD through business development activities, including support of proposal development, budget development and bid defense meetings; in some instances, leads proposal development and participates in bid defense meetings
- Participate in cross-functional task forces and organizational initiatives.
- Supervise and act as a guide and mentor to junior staff
- Support other organizational activities as needed (e.g., closely collaborate with other project collaborators such as clinical operations, data management, biostatistics, and data analysts; contribute to development o


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