Senior Clinical Scientist

Fortrea; United States; Remote; USD 110,000 - 130,000; Full time

Job summary

A leading company in clinical development is seeking a Senior Clinical Scientist. The role involves collaboration with medical and regulatory teams, input on clinical protocols, and requires significant experience in scientific research. The position, available remotely, offers a competitive salary and benefits, aimed at seasoned professionals in the clinical field.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

401(k)

PTO/FTO

Bonuses

Qualifications

• 10-12 years of experience with a Bachelor's, 4-6 years with a Master's, or Doctorate.
• Fluent in English with strong data interpretation skills.
• Knowledge of GCPs and regulatory guidelines.

Responsibilities

• Providing scientific input into protocols and development plans.
• Collaborating with teams to address complex scientific and regulatory issues.
• Writing and reviewing scientific documents like protocols and reports.

Skills

Data Interpretation

Regulatory Knowledge

Education

Bachelor's degree in scientific field

Master's degree

PhD

Job description

Join to apply for the Senior Clinical Scientist role at Fortrea.

The Clinical Scientist (CS) provides ongoing in-depth analysis and scientific input into the development and execution of protocols and clinical development plans. This role involves working with the medical/scientific/regulatory team to solve a wide range of medical, scientific, clinical, and regulatory problems, especially for early clinical trials.

Key Responsibilities include:

• Providing scientific input into protocols and development plans.
• Staying current with scientific developments through participation in meetings and courses.
• Collaborating with teams to address complex scientific and regulatory issues.
• Maintaining affiliations with scientific communities.
• Writing and reviewing scientific documents such as protocols, reports, and manuscripts.
• Providing scientific rationale for including biomarkers in studies.
• Participating in study meetings and supporting safety data review.
• Supporting process improvements and documentation standards.
• Other duties as assigned.

Minimum Qualifications:

• Bachelor’s degree in a scientific field with 10-12 years of experience, or a Master’s with 4-6 years, or a PhD.
• Knowledge of GCPs and regulatory guidelines.
• Strong data interpretation skills.
• Fluent in English.

Experience:

• Up to 15 years in related fields such as medical, clinical, pharmaceutical, or research.

Physical Demands and Work Environment:

• Office environment, with occasional overtime and travel (<10%).

Position is remote in the US or UK. Not eligible for sponsorship.

Salary range: $110,000 - $130,000 USD. Benefits include medical, dental, vision, life insurance, 401(k), PTO/FTO, and bonuses. Application deadline: June 9, 2025.