Clinical Scientist, eCOA Neuroscience

Clario

95d

About The Position

We are seeking an experienced and scientifically driven Clinical Scientist to serve as the external-facing clinical representative for international clinical trials. In this role, you will independently manage the scientific and operational aspects of assigned studies, ensuring scientific integrity, clinical quality, and stakeholder alignment from study start-up through closeout. You will collaborate closely with sponsors, investigators, and cross-functional teams to deliver high-quality clinical outcomes while maintaining compliance with GCP and study protocols.

Requirements

• Bachelor’s degree in life sciences or a related field required; graduate degree preferred.
• 5+ years of experience in the clinical research industry; CRO or biopharmaceutical sponsor background preferred.
• 3+ years in a clinical scientist, trial science lead, site educator, or similar client-facing scientific role.
• 4+ years administering and/or training on rating scales in sponsored clinical research; pediatric neurodevelopmental scale experience strongly preferred.
• Strong knowledge of study endpoints, research methods, and basic/intermediate statistics.
• Proven leadership skills with the ability to influence, negotiate, and motivate cross-functional teams.
• Excellent problem-solving, decision-making, and critical thinking skills.
• Skilled communicator, able to tailor presentations to diverse audiences and present effectively in front of large groups.
• Proficient in MS Word, Excel, PowerPoint, with the ability to produce detailed reports and presentations.
• Fluent in English; additional languages a plus.
• Strong understanding of Good Clinical Practice (GCP).
• Ability to travel internationally as needed (must maintain documentation for travel eligibility).
• Based in or able to work from the United States (remote/hybrid).

Responsibilities

• Serve as the clinical lead for assigned projects, managing scientific oversight and ensuring all analyses, remediations, and communications uphold scientific integrity.
• Participate in internal and external project meetings, including sponsor calls and Investigator Meetings.
• Monitor study metrics, identify outliers, address issues proactively, and present dashboards and corrective actions to sponsors.
• Lead calibration of clinical teams, conduct rater training events, and oversee remediations per study-specific training plans.
• Provide scientific guidance and support to internal teams and external stakeholders, addressing WCG scoring or feedback inquiries.
• Develop project deliverables, including scale verification, electronic form design, and training materials for live or online sessions.
• Partner with Business Development to evaluate potential studies and RFPs as needed.
• Build and maintain relationships with external consultants, key opinion leaders, and clinicians.
• Contribute to research and publication initiatives, presenting findings through peer-reviewed journals, conferences, or other professional venues.
• Support process improvement initiatives by developing or refining SOPs, work instructions, and guidelines to ensure compliance with SOP/GCP requirements.

Benefits

• Competitive compensation.
• Medical, dental, and vision coverage starting Day 1.
• Flexible and paid time off.
• Remote and hybrid work options.
• Employee assistance and wellness programs.

What This Job Offers

• Career Level: Mid Level
• Education Level: Bachelor's degree
• Number of Employees: 5,001-10,000 employees