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Director Real World Evidence Rwe Jobs in Atlanta, GA

Tempus

Senior Scientist R&D

Atlanta, GA · On-site

$94K - $135K/yr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for ...

UCB

Global Head of Data Acquisition (US)

Atlanta, GA

Who you will work with You will collaborate across Development, Medical, Real-World Evidence, Commercial, Integrated Insights, the Global Data Office, and Digital Technology teams. Partnerships with ...

micro1 AI

Director of Biostatistics

Sandy Springs, GA · Remote

$60 - $100/hr

Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work

micro1 AI

Director of Biostatistics

Atlanta, GA · Remote

$60 - $100/hr

Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work

micro1 AI

Director of Biostatistics

South Fulton, GA · Remote

$60 - $100/hr

Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required -- your domain knowledge is what matters. Scope of Work

Merck & Co.

Sr. Manager, Medical Field

Atlanta, GA · On-site

$178.50 - $210/hr

At the local level, identify opportunities for collaboration in Real World Evidence with internal ... and pharmacy directors is required. * Demonstrated ability and experience working cross ...

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Director Real World Evidence Rwe information

What is the difference between Director Real World Evidence Rwe vs Clinical Data Manager?

AspectDirector Real World Evidence RweClinical Data Manager
CredentialsAdvanced degrees (PhD, MD, or Master’s), industry certificationsBachelor’s or Master’s in life sciences, clinical research
Work EnvironmentStrategic, cross-functional teams, senior managementData collection, database management, clinical trial sites
Industry UsagePharmaceuticals, biotech, healthcare analyticsClinical research organizations, pharmaceutical companies

The main difference is that the Director Real World Evidence Rwe focuses on designing and leading real-world data studies to inform healthcare decisions, while the Clinical Data Manager handles the collection and management of clinical trial data. The Rwe director has a broader strategic role, whereas the Clinical Data Manager is more operational and detail-oriented.

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Director Real World Evidence Rwe jobs near you
Infographic showing various Director Real World Evidence Rwe job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.

Senior Scientist R&D

Tempus

Atlanta, GA • On-site

$94K - $135K/yr

Full-time

Re-posted 21 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

Senior Scientist, Molecular Assay Development in R&D

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

We are looking for a Senior Scientist within the Molecular Assay Development group to co-lead the design and development of assays in support of IVD & CDx programs. In this role you will lead projects with staff scientists that lead the wet lab efforts during development and guide documentation specialists to assist in IVD documentation efforts. You will rise to the challenge of designing, supporting and documenting V&V studies for molecular assays, ensure project deliverables are compliant with applicable regulations, and provide technical reports to support FDA submissions. You are expected to collaborate cross-functionally with members of technology development, bioinformatics, quality control, regulatory affairs, and the clinical lab.

What you'll do:

  • Maintain overall knowledge of the assay characteristics

  • Provide scientific leadership to cross-functional teams

  • Manage and lead generation of R&D design documents

  • Lead validation team from project inception through launch including sample selection, hands-on laboratory validation, establishing workflow and SOPs, and authoring validation plans and summaries

  • Ensure activities are consistent with project critical path and respond appropriately to changing priorities

  • Assist in developing and tracking project budgets

  • Design assay performance specifications

  • Ensure assay development process meets milestones and timelines

  • Troubleshoot and solve technical issues

  • Maintain compliant laboratory documents and procedures

  • Proactively improve efficiency, quality and effectiveness of R&D efforts

Qualifications:

  • PhD in Nucleic Acids Biochemistry, Molecular Biology, or related field with 3+ years industry experience -or- MS with industry experience commensurate with requirements

  • Demonstrated leadership capabilities in assay development in an FDA regulated environment for IVD products under design controls

  • Strong technical expertise and hands on experience with nucleic acid technologies with a preference towards NGS, PCR, and qPCR techniques

  • Proven ability to apply principles of quality control and quality assurance to development activities

  • Strong understanding of FDA, EUA, and other global regulatory requirements

  • Demonstrated technical and project leadership expertise

  • Good organization skills, detailed oriented mindset

  • Ability to thrive in a fast paced environment

  • Team driven


$94,000.00-$135,000.00

The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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