Research Scientist – Patient-Centered Outcomes, In-Trial Research

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Act as the independent Principal Investigator for various projects.

• Supervise all elements of project delivery and assign project management duties to junior scientific staff.

• Assume scientific responsibility for project completion while offering strategic guidance.

• Employ optimal methodologies to fulfill research requirements and manage a significant project portfolio.

• Drive scientific innovation and deliver high-quality scientific outputs.

• Perform both qualitative and quantitative scientific analyses.

• Showcase scientific findings in peer-reviewed journals and at professional conferences.

• Provide scientific guidance and leadership to team members.

• Design and execute scientific studies and communicate results directly to clients.

• Counsel colleagues on study design and execution.

• Contribute to publications, presentations, workshops, advisory boards, and meetings with the FDA.

• Cultivate and maintain relationships with clients.

• Advise clients on scientific methodologies and strategic plans.

• Assist clients in preparing for and participating in regulatory meetings.

• Generate proposal leads, write proposals, oversee proposal development, and secure sales.

• Achieve an annual target utilization rate of 60%, unless otherwise specified.

• Manage internal timelines, project budgets, scope adjustments, and legal and contracting matters.

• Develop and deliver internal scientific training sessions.

• Adhere to SOPs and Evidera/PPD standards.

• Support the development of new products and scientific innovations.

⛳️ Requirements

• Ph.D. in life sciences or social sciences with over 3 years of relevant experience, or a Master’s degree in a related field with 5–7 years of experience.

• An equivalent combination of relevant education, training, and/or experience may also be considered adequate.

• Proficiency in using Computer-Assisted Qualitative Data Analysis Software (CAQDAS) like Atlas.ti, NVivo, MAXQDA, or Dedoose.

• Experience in analyzing patient experience data, including interviews, surveys, and clinical outcome assessments (COA).

• Proven ability to manage multiple projects simultaneously.

• Strong understanding of qualitative research principles and familiarity with qualitative research within clinical trials.

• Extensive knowledge of qualitative methodologies.

• Advanced comprehension of operational and logistical challenges associated with in-trial research.

• Excellent communication and scientific writing skills.

• Strong analytical and problem-solving capabilities.

• Ability to independently oversee, manage, and/or lead project-related tasks while delegating effectively.

• Proficient in managing client relationships.

• Capable of multitasking in a collaborative environment.

• Experience in the pharmaceutical or consulting sectors is preferred.

• Familiarity with clinical research settings is advantageous.

🏝️ Benefits

• Fully remote work arrangements.

• Opportunities for collaboration and professional development.

• Global team atmosphere.

• Commitment to passion, innovation, and scientific excellence.

• Opportunities to contribute to scientific publications, presentations, workshops, advisory boards, and FDA meetings.

• Access to professional and scientific training and development.