72 applicants

Company

RTI International · 5 hours ago

Senior Scientist in Real-world Data

United States

Full-time

Remote

Senior Level, Lead/Staff

$200K/yr - $247K/yr

12+ years exp

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ConsultingEducation

Culture & Values

No H1B

U.S. Citizen Only

Hiring Manager

Kelly Vester

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Responsibilities

Lead proposals and projects as project director / principal investigator or major task leader of significant scope, scale and impact that contributes to the expansion of business across practice area, business unit and the institute’s project portfolio and client offerings.

Lead and support business development and marketing efforts activities including meeting with prospective clients and coordinating work with internal teams and external partners to monitor proposal and project deliverables, staffing, scope of work, costing, and scheduling.

Generate business opportunities by leveraging existing work for future work and though networking, professional relationships, and reputation as an expert, specifically in the field of RWD/RWE, epidemiology, informatics, and/or advanced analytics

Expand proposal and project capacity as a leader and mentor in developing talent and upskilling staff in RWD/RWE and distributed data approaches.

Guide teams in design and implementation of best practices, including research in drug safety and efficacy, and in the use of distributed data models.

Oversee implementation and use of common data models.

Define and develop research and programs to address key scientific issues while supporting a strong, consistent, and sustained revenue base.

Proactively identify and solve complex problems that impact the management and direction of the business

Successfully develop and implement plans to build internal capacity by serving as a senior advisor on data modernization and data strategy and associated digital strategy to support RWE and hybridized data solutions.

As a technical expert, write and review proposals or portions of other colleagues’ proposals to obtain funding from a broad range of clients and funding agencies.

Investigate and advise regarding feasibility for the most complex and high revenue projects. Serve as a technical expert and participate actively in the scientific and peer community and across a broad group of clients.

Prepare and deliver presentations at professional conferences and client meetings; write articles for scientific journals nad other publications.

Through the careful review of reports, patents, literature and other data, maintain an up-to-date comprehensive understanding of the latest developments in the technical field as it pertains to the scope of responsibility.

Actively participate in professional societies working with people outside the institute.

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

EpidemiologyPharmacoepidemiologyInformaticsReal-world evidence (RWE)Clinical researchData integrationLinkage of data typesProposal writingHealthcare domain expertisePublic health domain expertiseEHR dataClaims dataRegulatory researchFDA regulationsASTP/ONC policyCollaboration skills

Required

Doctoral degree in epidemiology, biostatistics, informatics, public health or related field and 12 years’ related experience with a focus on real-world evidence.

Ability to manage multiple priorities and deliver on tight and competing deadlines.

Strong interpersonal and collaboration skills - oral, written communication, and presentation skills.

Experience writing/responding to requests for proposals (RFPs) or other equivalent opportunities within the subject area.

Domain expertise in healthcare and/or public health.

Experience representing RWE and surveillance results to a range of parties, clients, or audiences.

Technical expertise in epidemiologic study design for surveillance, integration of disparate data types, appropriate use of linkage and mapping for RWD and common data models.

Awareness of the role of RWD in surveillance and regulatory research, and understanding of the policy landscape, including FDA regulations and ASTP/ONC policy for electronic health data.

Ability to anticipate problems and develop contingencies before issues arise (i.e. staffing, budget, or technical).

Demonstration of the RTI Values and Lead Forward behaviors.

To qualify, applicants must be legally authorized to work in the United States, and should not now, or in the future, require visa sponsorship.