Program Manager, Real-World Evidence (Epidemiologist) at Stryker

Newbury, England, United Kingdom

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Medical Devices, HealthcareIndustries

Requirements

Degree required (PhD preferred)
8+ years relevant experience in epidemiology, pharmacoepidemiology, and/or observational research in academia, a contract research organization, or the medical device or pharmaceutical industry
Hands-on experience with healthcare real-world data (RWD) sets such as patient registries, electronic medical records, hospital billing data, and insurance claims databases
Basic understanding of the clinical evidence needs in the global regulatory environment for clinical investigation, clinical evaluation, post-market clinical follow-up, and product ratings of medical devices and technologies that can be addressed using RWD
Sophisticated understanding and ability to analyze and interpret quantitative data, together with working knowledge of RWE/observational study design and methodology
Preferred: Strong knowledge of standard statistical software (e.g., SAS, R, Stata) and demonstrated ability to collaborate closely with statistical programmers
Preferred: Experience authoring study protocols, study reports, conference abstracts, and peer-reviewed publications using RWD
Well-developed interpersonal skills and the ability to work well independently as well as with colleagues and customers
Strong organizational skills, with ability to effectively and efficiently handle multiple tasks simultaneously, with precision, and to adapt to changes in responsibilities and workloads

Responsibilities

Provide strategic insight to evidence required by cross-functional project teams focused on market access or sustaining product portfolios, requiring global clinical insight into launch strategies across multiple regions
Manage planning and communication with cross-functional teams to ensure proper execution and conduct of the clinical studies, leveraging collaborators and stakeholders
Lead the design and execution of RWE studies in close collaboration with internal stakeholders from Clinical Strategy, Medical Affairs, Regulatory, HEOR, and Commercial
Ensure scientific rigor and serve as a methodology expert for RWE generation; select and implement appropriate analytic methods aligned to research needs
Author and/or oversee development of study protocols, reports, abstracts, and peer-reviewed publications using RWD and collaborate cross-functionally to integrate RWD into global publication strategies
Collaborate closely with data management and biostatistics functions to ensure data quality and deliver robust data analyses utilizing scientifically valid and accepted methodology for RWD
Conduct feasibility assessment of relevant data sources for specific devices and indications to ensure data is fit-for-purpose
Collaborate with academic institutions, health systems, registries and/or other health data partners to identify additional real-world data sources for medical device evidence generation
Ensure quality and performance standards for RWE projects are realistic and attained, and studies are conducted in line with quality/compliance framework
Identify areas of improvement with RWE processes and procedures, develop and implement best practices, and work to improve efficiencies and effectiveness
Participate in cross-functional and cross-divisional initiatives regarding RWE
Oversee and manage the design and execution of multiple RWE studies to support clinical evidence needs
Execute on key RWE deliverables, establish standards and best practices for RWE study design and reporting, and support the integration of real-world data sources as an essential part of the clinical evidence generation strategy for Stryker’s product portfolio

Skills

Key technologies and capabilities for this role

Real-World EvidenceRWE Study DesignEpidemiologyRWD AnalysisStudy ProtocolsBiostatisticsHEORClinical StrategyData ManagementPeer-Reviewed PublicationsFeasibility AssessmentAnalytic Methods

Questions & Answers

Common questions about this position

What is the work arrangement for this role?

The position offers a hybrid work flexibility.

What degree and experience are required for this position?

A degree is required with a PhD preferred, along with 8+ years of relevant experience in epidemiology, pharmacoepidemiology, and/or observational research in academia, a contract research organization, or the medical device or pharmaceutical industry.

What hands-on experience with real-world data is needed?

Candidates need hands-on experience with healthcare real-world data sets such as patient registries, electronic medical records, hospital billing data, and insurance claims databases.

What salary or compensation does this role offer?

This information is not specified in the job description.

What makes a strong candidate for this Program Manager role?

Strong candidates will have a PhD preferred, 8+ years in epidemiology or observational research, hands-on experience with RWD sets, and expertise in designing and executing RWE studies while collaborating cross-functionally.

Stryker

Develops and manufactures medical devices and equipment

About Stryker

Stryker develops and manufactures medical devices and equipment aimed at improving patient care and surgical efficiency. Their products include surgical tools, neurotechnology devices, and orthopedic implants, which are sold directly to hospitals and clinics. Stryker stands out from competitors by focusing on high-quality products and a commitment to advancing healthcare solutions. The company's goal is to enhance the overall healthcare experience for both patients and medical professionals.

Kalamazoo, MichiganHeadquarters

1941Year Founded

$423.3MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Medical & prescription plans

Supplemental health benefits

Flexible Spending accounts

Employee Assistance Program

Short-term & long-term disability

Tuition reimbursement

401(k) plan

Employee Stock Purchase Plan

Risks

Integration challenges from acquisitions may strain Stryker's resources.

Rapid tech advancements risk obsolescence of Stryker's current products.

Regulatory scrutiny on acquisitions could delay Stryker's market entry.

Differentiation

Stryker's acquisitions enhance its minimally invasive surgical solutions portfolio.

Entry into the peripheral vascular segment diversifies Stryker's market presence.

Stryker's focus on AI integration boosts diagnostic accuracy and operational efficiency.

Upsides

Growing demand for minimally invasive solutions aligns with Stryker's strategic acquisitions.

The orthopedic implants market growth benefits Stryker's expanding product line.

Stryker's acquisition of Inari Medical positions it in a high-growth vascular market.

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