Research Protocol Associate at Mayo Clinic

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.

Benefits Highlights

Medical: Multiple plan options.
Dental: Delta Dental or reimbursement account for flexible coverage.
Vision: Affordable plan with national network.
Pre-Tax Savings: HSA and FSAs for eligible expenses.
Retirement: Competitive retirement package to secure your future.

Responsibilities

Participates in components of the clinical trial development, implementation, maintenance, and completion process as directed. Responsibilities may include but are not limited to: assisting with protocol/clinical research development and maintenance including gathering regulatory documents, drafting the informed consent, developing clinical trial budgets, identifying/coordinating study logistics/approvals and protocol modifications. Must be able to work in a complex environment and exercise good judgment in ambiguous situations. Must possess excellent problem-solving skills, oral, written, communication and interpersonal skills, and be comfortable interacting with individuals at all levels internal and external to Mayo Clinic. Participates on projects as assigned. Provides input to standard operating procedures and working instructions.

This vacancy is not eligible for sponsorship/we will not sponsor or transfer visas for this position. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program.

Qualifications

Qualifications:

A bachelor’s degree is required OR associate degree or completion of college diploma program or certificate program with 2 years experience in the clinical research setting or related field.

Additional Qualifications:

Must be proficient in the use of computers, Microsoft applications.

Familiar with research systems, experience leveraging tools and technology. Prefer previous experience with regulatory documents.

Experience working remote, regulatory and quality assurance experience, working knowledge of Florence and Redcap system, experience with continuing review, close out, and final report submissions, ability to regularly meet deadlines, and ability to project manage the regulatory maintenance of clinical trials.

This role requires attention to detail, a sense of urgency to follow-up on tasks, professional demeanor and guidance, a desire for teamwork and excellence that supports bringing new studies to patients by providing white glove customer service to study sponsors and physicians.

Comfort learning new data systems and contributing to process improvements is key to success in this role.

Exemption Status

Nonexempt

Compensation Detail

$24.07 – $34.95 /hour; Education, experience and tenure may be considered along with internal equity when job offers are extended.

Benefits Eligible

Yes

Schedule

Full Time

Hours/Pay Period

Schedule Details

8 hours per day during core business hours between 7:00 am – 6:00 pm. Working hours support staff across US time zones. This position is 100% remote and available to candidates within the US.

Weekend Schedule

N/A

International Assignment

Site Description

Just as our reputation has spread beyond our Minnesota roots, so have our locations. Today, our employees are located at our three major campuses in Phoenix/Scottsdale, Arizona, Jacksonville, Florida, Rochester, Minnesota, and at Mayo Clinic Health System campuses throughout Midwestern communities, and at our international locations. Each Mayo Clinic location is a special place where our employees thrive in both their work and personal lives. Learn more about what each unique Mayo Clinic campus has to offer, and where your best fit is.

Equal Opportunity

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, protected veteran status or disability status. Learn more about the “EOE is the Law”. Mayo Clinic participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee’s Form I-9 to confirm work authorization.

Recruiter

Chelsea Crosby

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