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

This is a fully remote position, open to applicants in United Kingdom, +6 more countries.

📋 Description

• Act as the independent Principal Investigator for various projects while overseeing all elements of project execution.

• Assign project management responsibilities to junior scientific personnel.

• Assume scientific accountability for project outcomes and offer strategic consultancy.

• Utilize advanced scientific methodologies, primarily qualitative and partially quantitative.

• Share scientific findings in peer-reviewed publications and at industry conferences.

• Provide scientific direction and create high-quality scientific outputs.

• Advise on and execute methods and scientific innovations within project frameworks and designs.

• Create and present scientific studies and outcomes directly to clients.

• Support team members in study design and execution.

• Build and sustain relationships with clients.

• Counsel clients on scientific methodologies and strategies.

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

• Generate proposal leads, draft proposals, oversee the proposal writing process, and successfully close sales.

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

• Oversee internal timelines, budgets, staff hours, scope adjustments, legal, and contracting matters.

• Develop and deliver internal scientific training sessions.

• Adhere to SOPs and Evidera/PPD standards.

• Contribute to new product development and scientific innovation initiatives.

⛳️ Requirements

• PhD in a life sciences or social sciences field with over 3 years of relevant experience.

• Master’s degree in a life sciences or social sciences discipline with more than 5-7 years of relevant experience.

• A combination of suitable education, training, and/or directly related experience may be deemed acceptable.

• Proficiency in Computer-Assisted Qualitative Data Analysis Software (CAQDAS) such as Atlas.ti, NVivo, MAXQDA, Dedoose, etc. is essential.

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

• Proven ability to manage multiple projects simultaneously is necessary.

• Previous experience in pharmaceutical or consulting firms is preferred.

• Familiarity with working in a clinical research setting is advantageous.

• Strong grasp of qualitative research principles and experience with qualitative research in clinical trials.

• Comprehensive knowledge of qualitative methodologies.

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

• Well-honed communication skills and proficiency in scientific writing.

• Strong analytical and problem-solving capabilities.

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

• Competence in managing client relationships.

• Ability to collaborate effectively and multitask efficiently.

🏝️ Benefits

• Global team atmosphere.

• Opportunities for collaboration and professional development.

• Chance to contribute to scientific excellence and innovative breakthroughs.