Responsibilities

Executes the overall management of the clinical trial implementation, maintenance, and completion process in collaboration with protocol development team. Responsibilities may include but are not limited to coordination of the protocol/clinical research documents and/or the ongoing management of pre-written documents through the development; writing of the informed consent document; coordination of study logistics/obtaining 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. Provides consultative guidance regarding regulatory and policy requirements to physicians, study staff, and external sponsors. 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. 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. Active member on committees and task forces and participates on projects as assigned. Writes and provides input to standard operating procedures and working instructions. Develops and carries out staff training and mentoring as necessary.

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.

This position will accept applications until 01/10/2025.  This deadline may be extended if the necessary candidate pool is not met by this date.

Qualifications

Qualifications: 

Bachelor's with at least 2 years of experience in clinical research or related field OR associate degree or completion of college diploma program with 4 years' experience in the clinical research setting or related field. 

Additional Qualifications: 

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

License or Certification: 
SoCRA or ACRP certification preferred.

Exemption Status

Nonexempt

Compensation Detail

$27.55 - $41.37 / hour

Benefits Eligible

Yes

Schedule

Full Time

Hours/Pay Period

80

Schedule Details

Monday-Friday 8:00am-5:00pm Eastern. This position is 100% remote; can work from anywhere in the U.S.

Weekend Schedule

NA

International Assignment

No

Recruiter

Stephanie Brackey