Medical directors of Oncology Clinical Research—Salt Lake City

TANNER & ASSOC INC; Salt Lake City (UT); On-site; USD 160,000 - 220,000; Full time

Job summary

A leading company in the biotech sector is recruiting Medical Directors of Oncology Clinical Research in Salt Lake City. This role involves managing clinical trials, ensuring compliance with regulations, and contributing strategically to oncology programs. Candidates must possess a strong background in drug development and oncology, with excellent analytical and communication skills.

Qualifications

• At least 5 years of drug development experience.
• Prior clinical trial experience in oncology preferred.
• Strong technical knowledge of oncology and clinical trial processes.

Responsibilities

• Design clinical experiments, draft protocol summaries, and provide input for protocol development.
• Oversee key clinical trials and provide medical oversight for Phase I-III.
• Analyze and interpret data, presenting results clearly.

Skills

Drug development experience in Oncology

Problem solving

Communication skills

Education

M.D. with board certification in hematology/oncology or a PhD, PharmD

Job description

Medical Directors of Oncology Clinical Research—Salt Lake City

Tanner and Associates is recruiting several Medical Directors of Oncology Clinical Research for major biotech companies located in San Francisco, Los Angeles, Salt Lake City, and New Jersey. Candidates can be based in any of these locations.

Requirements:

Seeking Medical Director/Clinical Scientist with drug development experience in Oncology. Candidates should have an M.D. with board certification or eligibility in hematology/oncology, or a PhD, PharmD with at least 5 years of drug development experience. Prior clinical trial experience in oncology is preferred. Candidates must be proactive problem solvers and able to work independently.

Responsibilities include designing, implementing, analyzing, and interpreting clinical trials from phase I-III. The role involves contributing to the strategic direction of Oncology programs, including trial design, analysis, and dissemination of results. Building and maintaining relationships with investigators, regulatory authorities, and collaborating companies is essential.

Responsibilities:

Design:

• Design clinical experiments, draft protocol summaries, and provide clinical input for protocol development.
• Develop initial clinical designs for future trials, collaborating with research, biostatistics, regulatory, and other teams.
• Participate as a key member of the Clinical SubTeam, contributing to clinical development strategies.

Implementation:

• As Medical Monitor, oversee key clinical trials in accordance with ICH/GCP guidelines.
• Partner with Data Management for CRF design, data analysis, and quality assurance.
• Provide medical oversight for Phase I-III trials, serving as the primary Clinical Science contact and liaison for clinical operations and CROs.
• Conduct regular clinical reviews and collaborate on safety monitoring plans.

Analysis and Interpretation:

• Analyze and interpret interim and final data, presenting results clearly internally and externally.
• Demonstrate strong technical knowledge of oncology and clinical trial processes.
• Maintain excellent communication skills, both written and verbal.