Clinical Safety Director - Oncology

Hobson Prior; Trenton (NJ); Remote; USD 100,000 - 125,000; Full time

Job summary

An established industry player is seeking a Clinical Safety Director who specializes in Oncology. This fully remote role will have you at the forefront of ensuring the safety of pharmaceutical products, leading a dedicated team while overseeing safety strategies and managing risk throughout the drug lifecycle. You'll collaborate with various departments, analyze clinical trial data, and interact with regulatory bodies to ensure effective risk management. If you're passionate about drug safety and have a strong background in oncology clinical studies, this could be the perfect opportunity to make a significant impact in the life sciences field.

Qualifications

• Medical degree required with experience in oncology clinical studies.
• Strong skills in drug safety and clinical trials management.

Responsibilities

• Lead a team ensuring the safety of pharmaceutical products.
• Analyze clinical trial data to identify safety concerns.

Skills

Drug Safety

Oncology Clinical Studies

Clinical Trials Management

Team Leadership

Education

Medical Degree (MD)

Job description

Consultant - Engineering at Hobson Prior

Hobson Prior is seeking a Clinical Safety Director specializing in Oncology. In this role, you will lead or be part of a team focused on ensuring the safety of pharmaceutical products. Your main tasks will include overseeing safety strategies, monitoring clinical studies, and managing risk. You will work closely with various departments to maintain the balance between benefits and risks throughout the drug's lifecycle. This is a fully remote working role based within the United States.

Responsibilities:

1. Lead a team responsible for the safety of pharmaceutical products.
2. Act as the main contact for safety issues within project teams.
3. Analyze data from clinical trials to identify safety concerns.
4. Review reports on adverse events for accuracy and relevance.
5. Interact with regulatory bodies to ensure effective risk management.
6. Develop strategies to manage risks throughout the product's lifecycle.
7. Coordinate resources to deliver safety evaluations on time.

Key Skills and Requirements:

1. Medical degree (MD).
2. Experience in drug safety, particularly in oncology clinical studies.
3. Strong skills in clinical studies, trials, and safety management.
4. Ability to coach and lead a team effectively.

Apply now

If you are interested in learning more or applying to this exciting opportunity, please click 'Apply' and upload a copy of your CV.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.