Protocol Development Specialist

Basic education, experience and skills required for consideration:

• Master’s degree with 1 or more years of relevant experience or a Bachelor’s degree with a minimum of 3 years of relevant experience.
• Relevant experience must include at least one of the following:
• Development and/or use of clinical research protocols
• Writing of research protocols and/or grants
• Regulatory work involving clinical protocols and development of informed consents

Preferred education, experience and skills for consideration:

• Doctorate in biology, other life science, public health or research related discipline with a familiarity of the following: oncology, epidemiology, biostatistics, clinical research, regulatory science, healthcare/medicine.
• A background or knowledge within research study/experimental design, medical terminology, informed consent/clinical trial screening processes, adverse event collection/reporting and clinical protocol review and approval process
• Experience writing clinical trial protocols.
• Experience with the development, implementation or execution of single or multi-center clinical research studies.
• Familiarity with federal regulations and guidelines pertaining to interventional and non-interventional clinical research, including studies done under IND applications.
• CCRP, ACRP or equivalent certifications are preferred but not required

City of Hope is committed to creating a diverse environment and is proud to be an equal opportunity employer.  All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, or status as a qualified individual with disability.