Clinical Scientist

About Clario

Clario is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with new technologies revolutionizing what’s possible. From new trial modes to faster and integrated evidence and findings, our innovative clinical trial solutions mean we can unlock better evidence.

What We Offer (USA)

• Competitive compensation
• Medical, dental, and vision insurance beginning Day 1 of employment
• Flexible work schedules
• Attractive PTO plan
• Engaging employee programs
• Remote working

Essential Duties and Responsibilities

To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

• External Facing Clinical Representative: Responsible for the independent clinical management of international clinical trials.
• Scientific Leadership: Own scientific responsibility and co-lead each assigned project, along with accountability for ensuring that the scientific integrity is maintained and all necessary analyses and remediations are conducted and effectively communicated.
• Meeting Participation: Actively participate in internal and external project meetings (e.g., weekly external client call, Investigators’ Meetings).
• Metric Review and Reporting: Review, monitor, and proactively address issues regarding study level metrics; present study dashboards to sponsors by reviewing data, any outliers or areas of concern, as well as any actions taken to address these concerns.
• Issue Resolution: Resolve clinical quality or training related issues.
• Team Calibration and Training: Responsible for the calibration of clinical team, conduct rater training events, and remediations as specified in the study-specific training plans.
• Stakeholder Support: Provide scientific support to external and internal stakeholders, leveraging strong communication and negotiation skills and strategies.
• Inquiry Response: Respond to and resolve external inquiries regarding WCG scoring or feedback.
• Internal Coordination: Communicate with all internal stakeholders and coordinate resources to meet project objectives.
• Deliverable Development: Assist with or take responsibility for the development of project deliverables (e.g., scale verification, electronic form development, training materials for in-person or online training, etc.).
• Business Development Support: Work with Business Development to review potential studies, RFPs, as needed.
• Relationship Building: Develop and nourish peer-to-peer relationships with external consultants, key opinion leaders, and clinicians, both regionally and in research areas of interest.
• Research and Publication: Actively participate in research and publication efforts and report research results externally through peer-reviewed journals, conferences, or other appropriate venues.
• Process Improvement: Identify the need for and contribute to the development of departmental and cross-disciplinary work instructions, process guidelines and standard operating procedures to ensure all processes and procedures meet SOP/GCP requirements.
• Software Proficiency: Proficient knowledge of MS Office, specifically Word, Excel, PowerPoint and the ability to produce detailed reports and presentations using these tools.
• Travel: Ability to provide documentation allowing international travel.
• Other Duties: Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.
• Attendance and Punctuality: Attendance and punctuality are essential functions of the position.

Education Requirements

• Graduate degree in a life science discipline or other field relevant to the business focus preferred, bachelor’s degree required.

Qualifications/Experience

• Clinical Research Experience: Five years of experience in the clinical research industry required; experience working for a biopharmaceutical sponsor or a clinical research organization preferred.
• Client-Facing Scientific Role: Minimum 3 years of experience as a clinical scientist, clinical trial science lead, clinical site educator/supervisor or similar role with client-facing scientific responsibilities.
• Rating Scale Experience: Minimum 4 years of experience with the administration and/or training of rating scales with practical knowledge of study endpoints as part of sponsored clinical research is required. (pediatric neurodevelopmental scale e