[Hiring] Clinical Scientist @Perspective Therapeutics

Role Description

The Clinical Scientist will work to develop protocols and informed consent documents for clinical studies as well as draft clinical scientific documents such as INDs, IBs, and other documents for FDA/EMA submissions. This individual also will be responsible for driving the medical monitoring process. The Clinical Scientist will have the scientific expertise necessary to design and deliver clinical studies and programs. This individual should have a comprehensive background in oncology and must be able to work independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation.

Qualifications

• Advanced or clinical degree preferred (e.g., RN, BSN, MSN, MS, PhD, PharmD, or MD in a relevant scientific discipline such as Pharmaceutical Sciences, Radiopharmacy, Oncology, Molecular Biology, Biomedical Sciences, or a related field).
• 3+ years of clinical research experience in biotech, pharmaceutical, or CRO settings, with a focus on oncology, nuclear medicine, or radiopharmaceuticals preferred.
• Hands-on experience with clinical trial design, protocol development, and regulatory submissions (IND, CTA, BLA, NDA).
• Experience with clinical data review, safety assessments, and translational research in oncology or targeted radiotherapy is highly desirable.
• Experience developing training materials for clinical sites and CRAs, as well as presenting at Investigator Meetings or Site Initiation Visits (SIVs).
• Prior engagement with KOLs, investigators, and regulatory agencies (e.g., FDA, EMA, Health Canada) is a plus.

Requirements

• Strong understanding of GCP, ICH guidelines, and regulatory requirements for drug development.
• Familiarity with clinical pharmacology, radiology, and imaging modalities (e.g., PET, SPECT, CT, MRI) in a clinical trial setting is a plus.
• Proficient in Medical Terminology and medical writing skills.
• Computer proficiency in basic database entry and graphics presentations.
• Exceptional verbal and written communication skills, with demonstrated ability to communicate complex scientific information to diverse audiences.
• Strong leadership skills with experience leading cross-functional project teams and fostering collaboration across departments.
• Strategic thinker with the ability to translate scientific insights into actionable clinical strategies.
• Highly detail-oriented with strong problem-solving skills; proactive in anticipating and resolving issues.
• Advanced proficiency in medical writing and technical documentation; skilled in preparing high-quality scientific and regulatory documents.
• Comprehensive knowledge of Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and the drug development process.
• Must be willing to travel up to 20% of the time. Both domestic and international travel may be required.

Benefits

• Equal employment opportunities to all employees and applicants for employment.
• Prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Work Environment

• Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.
• May be required to sit or stand for long periods of 8+ hours a day while performing duties.
• Must be willing to wear a variety of Personal Protective Equipment (PPE), including eye and hearing protection, as needed.
• Willingness to complete safety training within allotted timeframes, and work in a team-based environment.