Team Lead-Sr Research Protocol Specialist - Radiology Research

This is a hybrid role: Candidate must be able to come onsite for coverage rotation and onsite project work as requested, therefore must be within driving distance of Mayo Clinic Rochester campus. Position could include up to 30% onsite work.

Along with overseeing the overall management of the clinical trial development, maintenance, and completion process, this role involves collaborating on large, complex, multi-center, investigator initiated clinical research protocols/programs. The incumbent will be responsible to accurately apply investigators' scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements.

Other responsibilities/duties may include, but are not limited to:

Collaborate with industry partners throughout the study lifecycle process; Provide consultative guidance regarding regulatory and policy requirements to physicians, study staff, and external sponsors.

• Coordinate the writing of the protocol/clinical research documents and/or the ongoing management of pre-written research documents through the development/coordination of study logistics, obtaining approvals, verification of content to meet institutional, industry, and federal standards.
• Partner with multidisciplinary stakeholders' enterprise-wide and help them effectively navigate the clinical trials process. 
• Spearhead an ever-growing dynamic RPS team to shape the future of research. 
• Write, develop, and provide input to standard operating procedures and working instructions.
• Educate and serve as an expert resource for other research personnel.

May lead or participate as a member on committees, task forces and lead on projects as assigned.

Master’s degree with 2 years’ experience in the clinical research setting or related field.

OR bachelor’s with at least 4 years of experience in clinical research or related field.

OR associate degree as a clinical research professional with 6 years’ experience in the clinical research setting or related field.

Must be able to work in a complex team environment both as a member and a facilitator, able to manage multiple projects at various stages, work independently, and possess excellent problem-solving, oral, written, communication, and interpersonal skills.

Must be proficient in the use of computers and Microsoft applications. Project management experience required, show proficiency in research systems, excel in leveraging tools and technology, and be knowledgeable with reg docs, IRB submission, writing consent forms.

Note: Must be U.S. citizen, permanent resident, refugee or asylee. Visa sponsorship is not available for this position.

Why Mayo Clinic
Mayo Clinic is top-ranked in more specialties than any other care provider according to U.S. News & World Report. As we work together to put the needs of the patient first, we are also dedicated to our employees, investing in competitive compensation and comprehensive benefit plans – to take care of you and your family, now and in the future. And with continuing education and advancement opportunities at every turn, you can build a long, successful career with Mayo Clinic. You’ll thrive in an environment that supports innovation, is committed to ending racism and supporting diversity, equity and inclusion, and provides the resources you need to succeed.