Mayo Clinic Senior Research Protocol Specialist - Orthopedics in Rochester, Minnesota
Independently executes the overall management of the clinical trial implementation, maintenance, and completion process. Directs large, complex, multi-center clinical research protocols/programs. Accurately applies 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. Responsibilities may include, but are not limited to: coordinating the writing of the protocol/clinical research documents and/or the ongoing management of pre-written protocol/clinical research documents through the clinical trial development/implementation process; writing of the informed consent document; coordination of study logistics/approvals, verification of content to meet institutional, industry, and federal standards; communication with study sites, industry partners, and/or federal agencies; development of clinical trial budgets; and ensuring Mayo standards are adhered to and appropriate approvals have been obtained. Provides consultative guidance regarding regulatory and policy requirements to physicians, study staff, and external sponsors. May contribute to grant applications, abstracts/posters, and manuscripts. Must be able to work in a team environment both as a member and a facilitator, be able to manage multiple projects at various stages, and be able to work independently with occasional guidance from physician leadership or management. Must be able to work in a complex environment and to exercise good judgment in ambiguous situations under pressure. Must possess excellent problem-solving skills, oral and written communication and interpersonal skills, and be comfortable interacting with individuals at all levels internal and external to Mayo Clinic. Active member on committees and task forces and participates on projects as assigned. Writes and provides input to standard operating procedures and working instructions. Educates and serves as an expert resource for other research personnel.
A bachelor’s degree is required; masters preferred. Minimum five years of experience in a clinical research setting or related field required. Must be proficient in the use of computers, Microsoft applications, and databases. Experience with medical terminology preferred.
Project management experience required. SoCRA or ACRP certification preferred.
Exemption status Exempt
Education, experience and tenure may be considered along with internal equity when job offers are extended. The minimum salary every 2 weeks is approx $2170.40, based on a full-time position.
Benefits eligible Yes
Schedule Full Time
Hours / Pay period 80
Schedule details Monday-Friday
Mayo Clinic is located in the heart of downtown Rochester, Minnesota, a vibrant, friendly city that provides a highly livable environment for more than 34,000 Mayo staff and students. The city is consistently ranked among the best places to live in the United States because of its affordable cost of living, healthy lifestyle, excellent school systems and exceptionally high quality of life.
Category Clinical Labs and Research
Career profile Research
Job posting number 149926BR
Recruiter Jill Squier
As an Affirmative Action and Equal Opportunity Employer Mayo Clinic is committed to creating an inclusive environment that values the diversity of its employees and does not discriminate against any employee or candidate. Women, minorities, veterans, people from the LGBTQ communities and people with disabilities are strongly encouraged to apply to join our teams. Reasonable accommodations to access job openings or to apply for a job are available.
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