Protocol Development Specialist - Clinical Oncology

City of Hope; Irwindale (CA); Remote; USD 60,000 - 100,000; Full time

Job summary

Join a pioneering organization committed to transforming healthcare as a Protocol Development Specialist. In this fully remote role, you will collaborate with clinical researchers to craft and refine clinical research protocols, ensuring they meet regulatory standards and facilitate groundbreaking studies. Your expertise will be crucial in enhancing non-scientific sections of protocols and providing exceptional support throughout the protocol approval process. This is an exciting opportunity to contribute to innovative research that aims to change lives and advance medical science.

Qualifications

• Master's or Bachelor's degree with 3+ years of relevant experience.
• Experience in clinical research protocols and regulatory work.

Responsibilities

• Assist in developing and editing clinical research protocols.
• Collaborate with stakeholders for document development.

Skills

Clinical Research Protocols

Regulatory Knowledge

Document Development

Customer Service

Education

Master's Degree

Bachelor's Degree

Job description

Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope

We are dedicated to changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our faculty and staff are driven by a mission to contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

Position: Protocol Development Specialist (PDS)

Join City of Hope as a Protocol Development Specialist and play a vital role in cutting-edge research. Collaborate with clinical researchers under the guidance of the OCPD Senior Manager to develop, write, and edit diverse clinical research protocols. This position is fully remote.

Key Responsibilities:

1. Assist investigators in developing, writing, and editing clinical research protocol documents.
2. Collaborate with stakeholders for document development through various channels.
3. Expand non-scientific sections of protocols with minimal supervision.
4. Communicate with sponsors or academic partners for protocol templates and study facilitation.
5. Review and edit protocol background sections to ensure submission readiness.
6. Provide excellent customer service with timely responses in document production.
7. Develop or review informed consent documents.
8. Coordinate responses during the protocol approval process, interfacing with internal stakeholders.

Qualifications:

• Master's degree or Bachelor's degree with a minimum of 3 years of relevant experience.
• At least 1 year of relevant experience required.
• Experience with clinical research protocols.
• Experience in composing therapeutic research protocols.
• Knowledge of regulatory work related to clinical protocols and informed consent development.

Note: City of Hope employees' pay is based on work experience, qualifications, and work location.

City of Hope is an equal opportunity employer committed to diversity, equity, and inclusion. Click here to learn more.

To learn more about our comprehensive benefits, please click here.