
Senior Manager, Clinical Scientist
Posted Jun 24

Posted Jun 24
This is a fully remote position, open to applicants in United States.
• Delivers scientific and/or medical expertise for the clinical research components of the project.
• Engages in strategic meetings and advisory boards as the primary clinical research representative.
• Contributes medical and scientific insights to key project documents (e.g., product strategy documents, target product profile (TPP), protocols, submissions, etc.).
• Collaborates with internal and external stakeholders as well as key opinion leaders.
• Supports other members of the project team in various functional areas.
• Acts as the medical or scientific representative when interacting with investigators and CROs.
• Provides medical and scientific analysis of efficacy and safety data.
• Participates in discussions with regulatory authorities (e.g., FDA, EMEA meetings).
• Offers input for the project publication plan, liaises with commercial teams, and assists with launch activities as necessary.
• Creates and reviews abstracts and manuscripts produced by internal or external contributors.
• Medical Degree, PhD, or PharmD is required.
• A minimum of 2-4 years of experience in clinical development within a pharmaceutical, biotechnology, CRO, clinical training/practice, and/or academic setting.
• Experience in metabolic diseases (such as Diabetes, Obesity, NASH, NAFLD), Endocrinology (including CKD, CRF), and drug development related to Nutrition and Weight Management is advantageous.
• Board eligibility or certification is preferred.
• Proven ability to manage multiple and varied projects simultaneously.
• Demonstrated capability to build positive relationships and foster collaborations.
• Strong analytical abilities; strategic thinker, planner, and implementer.
• Solid scientific skills with a keen attention to detail.
• Familiarity with biostatistics is a plus.
• Capability to work independently with minimal supervision.
• Extensive experience with literature analysis and demonstrated technical writing skills in English.
• Excellent written and verbal communication skills in English.
• High proficiency in major Microsoft Office applications (i.e., Word, Excel, PowerPoint, Project).
• N/A
Worldwide Clinical Trials
ICON plc
Parexel
ICON plc
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