Research Protocol Associate
Research Protocol Associate
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
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 bachelors 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.
Required Experience:
IC
Employment Type
Full-Time
