Source Job

US Unlimited PTO

  • Developed and executed study protocols, analysis plans, and study reports.
  • Designed and managed epidemiological, biomarker and/or data science projects.
  • Planned, designed, and conducted analyses for internal and external decision making.

20 jobs similar to Associate Director of Real World Evidence

Jobs ranked by similarity.

US Canada

  • Develop client-ready deliverables including protocols, statistical analysis plans, and technical reports.
  • Manage the delivery of project components by collaborating with other staff members.
  • Contribute to development of proposals and presentations under guidance of senior team members.

Precision Medicine Group is a portfolio organization that helps its clients with sophisticated evidence synthesis projects. The company has a start-up culture with vision in its field.

Canada US

  • Develop client-ready deliverables such as study protocols, statistical analysis plans, and technical reports for health technology assessment submissions.
  • Manage project components by collaborating with team members to ensure timely delivery, financial performance, and high-quality outputs, while handling day-to-day client communications.
  • Provide mentorship and direction to junior researchers, contribute to business development proposals, and apply technical expertise in systematic reviews and indirect treatment comparisons like NMA and MAIC.

Precision Medicine Group is a global portfolio organization specializing in evidence synthesis for health technology assessments in the pharmaceutical industry. The company has a culture similar to a start-up, is well-funded, and prides itself on being a visionary leader in its field.

US Unlimited PTO

  • Participate in client calls alongside clinicians to communicate the latest research findings.
  • Analyze patient medical records, including data extraction and tracking of lab values.
  • Research, evaluate, and prioritize treatment options for individual cases.

Private Health Management (PHM) is a clinically sophisticated healthcare navigation firm, specializing in assisting clients to obtain the best care and outcomes when facing serious and complex medical conditions. They believe everyone should benefit from the latest science-backed insights.

US

  • Lead statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, analysis datasets.
  • Oversee external functional service providers to ensure timely and high-quality programming deliverables.
  • Drive the adoption of innovative programming technologies and workflows to enhance the efficiency of clinical data review, cleaning, reconciliation, and integration.

Recursion is a clinical-stage TechBio company decoding biology to radically improve lives. The company is advancing a portfolio of differentiated investigational medicines across its wholly owned and partnered pipeline. Recursion's platform infrastructure is anchored in Salt Lake City, Utah and Milton Park, Oxfordshire.

  • Lead population analytics to identify variation in clinical and economic outcomes.
  • Apply RWE and health economic modeling to prioritize population health initiatives.
  • Communicate clinical, quality, and economic insights to leadership.

AffirmedRx aims to improve healthcare outcomes by making pharmacy benefits easy to understand and accessible. They are committed to clarity in business practices and use state-of-the-art technology. The company values its team and believes in a culture where people thrive.

US

  • Contribute to the design of early/late-stage protocols across multiple therapeutic areas.
  • Develop and write statistical analysis plans, and perform statistical analyses for interim and final reports.
  • Support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy.

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, they focus on quality, professional development, and a supportive culture.

Europe

  • Perform ongoing clinical data review to ensure data quality, consistency, and completeness.
  • Identify discrepancies and raise/resolve queries in EDC systems.
  • Review patient data including eligibility, medical history, treatment, safety data, and outcomes.

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. They partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity and anticipate change.

US 3w PTO

  • Coordinate research studies and deliverables across the PTFI ecosystem.
  • Support study design and execution in partnership with PIs and laboratories.
  • Ensure datasets meet defined standards for analysis readiness and cross-omics integration.

The American Heart Association is dedicated to fighting cardiovascular diseases and stroke. With nearly a century of experience, they focus on breakthroughs in science, policy, and care to build healthier lives.

$44–$60/hr
US 4w PTO

  • Contribute to the design and planning of clinical and real-world evidence studies.
  • Create and maintain scientific and operational documentation and tools to support Oura’s clinical and real-world evidence studies.
  • Support data-driven insights generation through organizing, summarizing, and describing health-related data.

Oura's mission is to empower every person to own their inner potential. Their award-winning products help their global community gain a deeper knowledge of their readiness, activity, and sleep quality by using their Oura Ring and its connected app. As a quickly growing company focused on helping people live healthier and happier lives, they ensure that their team members have what they need to do their best work — both in and out of the office.

US

  • Lead end-to-end Clinical Data Management activities for assigned clinical studies.
  • Ensure clinical data are accurate, complete, consistent, and inspection-ready.
  • Drive proactive risk identification, issue escalation, and resolution across study teams and vendors.

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease, guided by core values and focused on innovation.

Europe

  • Represent the Biostatistics function for complex studies or at project level.
  • Independently contribute to design of early/late-stage protocols across multiple therapeutic areas and help draft protocols or amendments.
  • Develop and write statistical analysis plans and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

US

  • Accountable for all core SP deliverables (SDTM, ADAM, TFLs).
  • With IT, defines our programming environment and its validation.
  • Responsible for the development of standards, SOPs, and best practices.

Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. Mineralys is a fully remote company that appears to be mid-sized, offering a collaborative and fast-paced environment.

US

  • Provide statistical support for Phase I–IV clinical trials.
  • Participate in protocol development, study design, and sample size calculations.
  • Prepare and review Statistical Analysis Plans (SAPs), TLF shells, and randomization specifications.

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries with a mission to contribute to a healthier and safer world.

US

  • Serves as the senior health science & epidemiology leader among contract staff.
  • Administratively and professionally responsible for the planning, direction, and execution of contract team activities.
  • Conducts rigorous etiologic and exposure assessment research studies in working populations.

Advanced Technologies & Laboratories International, Inc. (ATL) offers expertise in various scientific and technical domains. While the job posting does not explicitly mention employee numbers or culture, it emphasizes professional growth and investment in employees.

US

  • Oversees all aspects of study site management to ensure patient safety and data quality.
  • Independently conducts all forms of site visits and prepares monitoring reports.
  • Communicates effectively with site personnel and Precision Project and Clinical Trial Management.

Precision Medicine Group is a company that works in clinical research. They are an equal opportunity employer that values diversity and inclusion.

US

  • Independently coordinate assigned study activities in compliance with protocols, SOPs, GCP, and regulatory requirements.
  • Manage scheduling and execution of virtual and home-based study visits, assessments, and follow-up activities.
  • Serve as a primary point of contact for research participants and caregivers, including Spanish-speaking populations

Synapticure provides instant access to expert neurologists, cutting-edge treatments and trials, and wraparound care coordination and behavioral health support in all 50 states through a virtual care platform. As a patient and caregiver-founded company, Synapticure is dedicated to transforming the lives of millions of individuals and their families living with neurodegenerative diseases.

Europe

  • Preparation of Initial Investigational New Drug (IND) applications and amendments.
  • Provide guidance and support to other in‑house units in the preparation or review of manuals, training guidelines, and similar documentation.
  • Serve as a resource for new medical writers, offering direction, feedback, and support as needed.

Theradex Oncology is a full-service CRO, conducting early and late-phase oncology trials in the U.S, Europe and Asia. Their focus is cancer, understanding the science behind each potential cancer therapy and the challenges of moving therapies from mice to man.

US

  • Author, review, and manage clinical, regulatory, technical, and medical documents including protocols, study reports, and regulatory submissions.
  • Ensure strategic alignment and consistency of scientific messaging across documents while maintaining compliance with global regulatory requirements.
  • Drive the end-to-end writing process, manage timelines, and lead cross-functional reviews to deliver high-quality, on-time deliverables.

Kiniksa Pharmaceuticals is a commercial-stage biopharmaceutical company developing and commercializing novel therapies for diseases with unmet need, focusing on cardiovascular indications. The company fosters a highly collaborative, patient-first culture led by accomplished life sciences leaders, empowering talented individuals to make a real impact.

US

  • Provide methodological and epidemiological advice on data analysis.
  • Identify appropriate analytical methods or statistical programs to address study objectives.
  • Prepare basic, statistically sound analyses for manuscripts intended for publication.

Advanced Technologies & Laboratories International, Inc. (ATL) provides advanced technology and laboratory services. They focus on occupational safety & health research, offering a collaborative environment.

US

  • Provide expert review of respiratory trial protocols.
  • Sense-check recruitment assumptions and identify practical barriers to enrolment.
  • Lend clinical and scientific credibility to prospect conversations.

Lindus Health is powering biology's century with faster, more reliable clinical trials. They have raised a $55M Series B and aim to transform how people develop treatments, so patients can access breakthrough treatments faster. The company values collaboration, fun, and creativity.