Clinical Scientist

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

📋 Description

• Act as an external-facing clinical representative with independent scientific responsibility for designated international clinical trials, serving as the main point of contact for clinical and scientific inquiries.

• Co-lead projects while maintaining accountability for scientific integrity, ensuring proper analyses, issue resolution, and effective communication with sponsors and internal stakeholders.

• Actively engage in both internal and external project meetings, including sponsor calls and investigator gatherings.

• Review, monitor, and proactively tackle study-level metrics; create and present study dashboards that highlight data trends, outliers, risks, and mitigation strategies.

• Address clinical quality, data integrity, and training-related challenges in accordance with study requirements and Good Clinical Practice (GCP) standards.

• Oversee the calibration of clinical teams, facilitate rater training sessions, and execute remediation activities based on study-specific training plans.

• Offer scientific guidance and support to internal teams, sponsors, and external partners utilizing effective communication, influence, and negotiation techniques.

• Handle and resolve external inquiries regarding Clario scoring methodologies or clinical feedback.

• Coordinate cross-functional resources to guarantee that project milestones and deliverables are achieved.

• Assist in the creation of project deliverables, including scale verification, electronic form development, and training materials for both in-person and virtual presentations.

• Support Business Development efforts by providing scientific insights for feasibility assessments and RFP submissions.

• Establish and nurture professional relationships with external consultants, key opinion leaders, and clinicians.

• Engage in research initiatives and share findings through publications, conferences, or other scientific forums.

• Aid in the development and ongoing enhancement of work instructions, process guidelines, and SOPs to ensure adherence to SOP and GCP standards.

⛳️ Requirements

• A bachelor's degree is required; a graduate degree in life sciences or a related discipline is preferred.

• A minimum of five years of experience in the clinical research sector, with prior experience in a CRO or biopharmaceutical setting being advantageous.

• At least three years of experience in a role as a clinical scientist, clinical trial science lead, or a comparable client-facing scientific position.

• Minimum of four years of practical experience in administering and/or training on clinical rating scales and study endpoints.

• A solid grasp of basic and intermediate research methodologies and statistics.

• Proven capability to manage multiple projects in a fast-paced environment.

• Demonstrated leadership through influence, coupled with strong problem-solving and independent critical-thinking abilities.

• Excellent written and verbal communication skills, with experience in presenting to diverse and large audiences.

• Proficiency in English; knowledge of additional languages is a plus.

• Strong understanding of Good Clinical Practice (GCP) guidelines.

• Willingness to travel internationally approximately 10–20% of the time and perform extended periods of computer-based work.

🏝️ Benefits

• Competitive salary

• Comprehensive medical, dental, and vision insurance

• 401(k) plan with company matching

• Generous paid time off and company holidays

• Flexible remote work options available within the United States