Mayo Clinic offers a variety of employee benefits. For additional information please visit Mayo Clinic Benefits . Eligibility may vary.
Position description
Independently directs large, complex, multi-center clinical research protocols/programs in collaboration with the principal investigator and in compliance with regulatory laws and institutional guidelines. In collaboration with the principal investigator, researches, develops, and submits to appropriate agencies the study protocol in support of research 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. Manages research activities and subject participation including screening, enrollment, and recruitment. Identifies, reviews, and reports adverse events, protocol deviations, or other unanticipated problems appropriately. Oversees and monitors research data to maintain quality. Performs administrative and regulatory duties related to the study as assigned. Applies statistical/analytical methods to studies and contributes to/authors/co-authors grant applications, abstracts/posters, and manuscripts. May present research results/abstracts internally and externally. Represents Mayo and principal investigator at meetings and in the administration of research protocols. Educates and serves as an expert resource for other research personnel that may include residents and fellows. In addition to technical duties above, this position serves as the working supervisor over study coordinators in a program or across multiple programs. Supervisory duties performed will vary based on the percentage of time dedicated to supervision.
Qualifications
Associate’s degree with 6 years’ experience in clinical research or related field OR Bachelor’s degree with 3 years’ experience in clinical research with primary responsibility in FDA regulated clinical trials OR Bachelor’s degree with 4 years’ experience in clinical research OR Relevant Master’s degree with 1 year of experience in clinical research.
Additional qualifications
One year supervisory or employee management experience preferred
Internal applicants should attach their three most recent performance appraisals.
License or certification
SoCRA or ACRP certification preferred.
Exemption status
Exempt
Compensation Detail
Education, experience and tenure may be considered along with internal equity when job offers are extended. The minimum pay rate is $2492.80 per 2 week pay period based on a full time FTE.
Benefits eligible
Yes
Schedule
Full Time
Hours / Pay period
80
Schedule details
Must be flexible to meet the business needs of the unit, including evening and weekend on-call responsibilities.
Weekend schedule
As needed (On call)
International Assignment
No
Site description
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.
Recruiter
Krista Ellis
EOE
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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