FSP Clinical Scientist III / Medical Science Liaison

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

📋 Description

• Deliver continuous comprehensive analysis and scientific insights to support the development and implementation of protocols and clinical development plans.

• Collaborate with the medical/scientific/regulatory team to address medical, scientific, clinical, and regulatory challenges.

• Act as a resource for the Medical Monitor by monitoring and evaluating study-specific safety data to detect safety trends.

• Serve as a liaison among the Medical Monitor, study sites, Fortrea project personnel, and Sponsors concerning protocol and study-related inquiries.

• Document, monitor, and follow up on issues related to the study.

• Assess and review CPS proposals, offering clinical and scientific support.

• Prepare study outlines and designs, providing guidance on early clinical development strategies.

• Establish and nurture relationships within the Fortrea and broader scientific community.

• Offer rationale and insights for incorporating biomarkers or other laboratory markers in Proof-of-Concept studies.

• Participate in Kick-off Meetings, SIVs/Investigator Meetings, and Team Meetings.

• Assist in training on key medical/scientific topics.

• Ensure that medical and safety matters discussed in team meetings are addressed by the Medical Monitor.

• Support CPS Medical Monitors in tracking and documenting Inclusion/Exclusion criteria and protocol-related questions and responses.

• Carry out other related responsibilities as assigned.

⛳️ Requirements

• A Doctor of Medicine (MD) degree is mandatory.

• Previous hands-on experience as a licensed physician (MD) in clinical practice is required.

• A minimum of 2+ years of hands-on experience as a licensed physician in clinical practice is preferred.

• Experience specific to Hereditary Angioedema (HAE) is essential.

• Demonstrated progressive responsibility within a CRO or Sponsor environment.

• Familiarity with GCPs and regulatory agency guidelines is required.

• Capacity to perform limited reviews of relevant literature and references and apply the findings effectively.

• Proficiency in data interpretation.

• Fluent in English for speaking, writing, and reading.

• At least 10+ years of experience in pharmaceutical and clinical research, including a minimum of 5+ years in a medical monitoring/medical data review position.

• Significant travel is required throughout the year.

• Must have authorization to work in the United States on a full-time basis.

• The company does not offer visa sponsorship now or in the future.

🏝️ Benefits

• Medical insurance.

• Dental insurance.

• Vision insurance.

• Life insurance.

• Short-term disability (STD).

• Long-term disability (LTD).

• 401(K).

• Paid time off (PTO) or Flexible time off (FTO).

• Company bonus where applicable.