Instagram
youtube
Facebook

Senior Clinical Manager, Targeted Alpha Therapy, Radiopharmaceutical - Fsp

5+ years
$145,000–$155,000 USD annually
10 July 31, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Senior Clinical Manager – Targeted Alpha Therapy (Radiopharmaceutical)

Location: Remote – United States or Canada
Category: Clinical Research
Experience Level: Senior (5+ years)
Compensation Range: $145,000–$155,000 USD annually
Job Type: Full-time
Work Mode: Remote


Job Summary:

Fortrea is hiring a Senior Clinical Manager with expertise in Oncology and Radiopharmaceuticals, particularly Targeted Alpha Therapy (TAT). This remote opportunity allows experienced professionals in the US or Canada to lead strategic protocol development, safety analysis, and clinical project execution within early-phase drug trials. The role demands scientific leadership in radiopharma and oncology while offering global exposure in clinical development.


Key Responsibilities:

  • Provide scientific input for early-phase protocol and clinical development plans

  • Review CPS proposals and draft study outlines/designs

  • Participate in safety reviews, data monitoring, and dose escalation meetings

  • Draft and review medical documents including synopses, protocols, and clinical development plans

  • Serve as liaison between sponsors, medical monitors, study teams, and clinical sites

  • Analyze and interpret clinical trial safety data (e.g., AEs, ECGs, lab results)

  • Assist with biomarker inclusion strategies for POC studies

  • Track, document, and support the resolution of protocol-related inquiries

  • Ensure timely SAE handling and documentation

  • Engage in SOP updates, documentation standardization, and process improvements

  • Attend kick-off meetings, investigator meetings, and training sessions


Required Skills & Qualifications:

  • Bachelor’s or Master’s degree in a scientific field (PhD preferred)

  • 4–6 years of experience in clinical, medical, pharmaceutical, or research environments

  • Mandatory: Experience in Radiopharmaceuticals and Oncology

  • Strong understanding of GCP and global regulatory guidelines

  • Proven expertise in study design, clinical site setup, and stakeholder communication

  • Ability to lead and contribute in cross-functional clinical teams

  • Excellent written and verbal communication skills


Perks & Benefits:

  • Competitive salary: $145,000–$155,000 USD

  • Remote flexibility for US and Canadian candidates

  • Full benefits: medical, dental, vision, life, STD/LTD

  • 401(k), ESPP, company bonus (where applicable)

  • Paid Time Off (PTO) / Flexible Time Off (FTO)

  • Access to leading global pharma and biotech companies

  • Opportunity to work on cutting-edge radiopharmaceutical therapies


Company Description:

Fortrea is a leading global Contract Research Organization (CRO) providing world-class clinical development solutions across 100+ countries. With a strong focus on oncology, radiopharmaceuticals, and early-phase trials, Fortrea partners with top pharmaceutical and biotech companies to accelerate breakthrough therapies to market.


Work Mode: Remote – Open to candidates in the US and Canada

Travel Requirement: Less than 50% (may require overnight stays)


Call to Action:

Are you ready to lead pioneering radiopharmaceutical trials in a global clinical environment? Join Fortrea’s remote team and shape the future of targeted alpha therapies.
Apply now to take the next bold step in your clinical research career.