Associate Director, Real World Evidence

Cytel

$120K — $150K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Advanced degree in Epidemiology, Biostatistics, Data Science, Pharmacology, Biochemistry, or related field; MPH, MBA, MD, PharmD, or PhD preferred.
  • 8-10 years of experience in consulting or real-world evidence study designs; experience in a health research environment is a must.
  • Prior management experience required to support team leadership.
  • Strong interpersonal, verbal, and written communication skills for effective client interactions.
  • Demonstrated critical thinking and problem-solving abilities, enabling effective decision-making.
  • Proven influencing skills to navigate complex client relationships.
  • Ability to manage multiple tasks effectively while maintaining attention to detail.

Responsibilities

  • Lead real-world evidence projects, including comparative effectiveness studies and healthcare cost studies.
  • Drive business development and marketing activities as a connection point for clients and proposals.
  • Engage in client conversations and project scoping to define project needs and solutions.
  • Enhance Cytel's visibility through external engagements like conferences, webinars, and publications.
  • Oversee department operations, ensuring adherence to organizational productivity and quality standards.
  • Plan and allocate resources effectively for project staffing and execution.
  • Mentor a proactive team of RWE consultants in analytic and study design backgrounds.

Benefits

  • Opportunities for professional growth and development.
  • Mentorship within a strong, collaborative team environment.
  • Exposure to high-profile projects and external visibility engagements.
  • Engagement in process improvement initiatives that impact quality and efficiency.
  • Access to a diverse and supportive workplace culture that values teamwork.
Full Job Description
Job Description

Key member of a team of consultants in the RWE department at Cytel, based in North America, responsible for initiating opportunities in collaboration with our business development partners, overseeing the drafting of proposals and overseeing the delivery team to ensure client satisfaction.

Responsibilities

Act as sr project lead in RWE projects using retrospective, including but not limited to comparative effectiveness studies, treatment patterns and healthcare cost and utilization studies, post-authorization studies (PASS), external control arms (ECA), target trial emulation (TTE), real-world data landscaping and feasibility studies, and development of integrated evidence generation plans for our pharmaceutical clients.

Contribute to growth via business development and sales & marketing activities in collaboration with other subject matter experts and business developers, by connecting to clients and leading proposals and RFIs.

Takes the lead on conversations with clients (assist with/provide demos, capabilities presentations, client conversations on project scoping, project issues). Undertake external visibility engagements (conference presentations, webinars, peer reviewed publications and white papers etc.) to increase recognition of Cytel RWE that leads to new business.

Ensure employees adhere to company policies and procedures and employees meet organization's expectations for productivity, quality, continuous improvement, and goal accomplishment.

Contribute to the operational, budgetary, and financial responsibilities and activities of the department, as directed by senior management.

Contribute or lead planning and allocating resources to effectively staff and accomplish the work and meet utilization goals. Provides leadership and management at the project level related to technical planning, execution and delivery. Fully independent for most projects and supports overall team management initiatives (e.g. recruiting, training/coaching)

Contribute through mentorship to a strong, proactive team of RWE consultants both with analytic and study design background.

Contribute or lead with process improvement initiatives to enhance speed, quality, efficiency, and output.

Foster a spirit of teamwork and unity among the team that allows for disagreement over ideas, conflict and expeditious conflict resolution, and the appreciation of diversity as well as cohesiveness, support, and working effectively together to enable success.

Qualifications

Education: advanced in Epidemiology, Biostatistics, Data Science, Pharmacology, Biochemistry, or other relevant scientific field. MPH, MBA, MD, PharmD or PhD are highly desirable.

Experience: 8-10 years' progressive experience in consulting, real-world evidence study designs and analytic methods or health research environment. Previous management experience required.

Skills:

Excellent interpersonal, verbal and written communication skills

Excellent critical thinking and problem-solving skills

Influencing skills

Ability to manage multiple and varied tasks and prioritize workload with attention to detail

Financial and business acumen

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