Clinical Research Coordinator Neurology

This position will support Neurology Research.

You are invited to explore an exciting career as Clinical Research Coordinator (CRC) where you will utilize your strengths in organization multi-tasking attention to detail compassion and communication. You will work closely with Physicians Clinical Study Teams and most importantly this fast-paced environment you will enjoy working independently to carry out your day and look forward to having the opportunity to work on a variety of clinical study opportunities some on the forefront of new treatments devices and cutting-edge science innovations. Our teams have expertise in many areas such as phlebotomy startup negotiations and drafting of initial consent forms so you focus on the core work allowing you the opportunity to have strong working relationships with study teams and patients. We encourage you to apply if you have previous CRC experience or other relevant experience in regulatory consenting animal science labs or direct patient care case management or healthcare customer service.

Essential Job Functions

• Independently coordinates complex clinical research protocols with minimal direction.
• Collaborates with research team to assess feasibility and management of research protocols.
• Screens enrolls and recruits research participants.
• Coordinates schedules and monitors research activities and patient participation.
• Identifies reviews and reports adverse events protocol deviations and other unanticipated problems appropriately.
• Manages monitors and reports research data to maintain quality and compliance.
• Provides education/training for others within the department.
• Performs administrative and regulatory duties related to the study and participates in other protocol development activities.

During the selection process you may participate in an OnDemand (pre-recorded) interview that you can complete at your convenience. During the OnDemand interview a question will appear on your screen and you will have time to consider each question before responding. You will have the opportunity to re-record your answer to each question Mayo Clinic will only see the final recording. The complete interview will be reviewed by a Mayo Clinic staff member and you will be notified of next steps.

Additional Information:

This position is onsite and may be eligible for telework 1-2 days per week after a patient and study assessment has been completed and deemed acceptable. While working remotely staff are expected to be onsite for essential study tasks. Staff must also successfully complete a 6-month training assessment demonstrate ability to work independently be reliable and exhibit efficiency and accuracy of completing tasks.

Travel expected between the Phoenix and Scottsdale campus dependent on patient needs.

Qualifications

Must meet one of the following:

HS Diploma with at least 5 years of clinical research coordination/related experience

Associates degree/college Diploma/Certificate Program with at least 3 years of experience

Associates in Clinical Research from an accredited academic institution without experience

Bachelors with at least 1 year of experience or completion of a Mayo Clinic-sponsored clinical research internship in lieu of 1 year of experience

Note - Experience should be in the clinical setting or related experience.

Visa sponsorship is not available for this position. This position is not eligible for F-1 OPT STEM extension.

Internal candidates are encouraged to attach their performance appraisals (1-3) if available.

Additional Experience and/or Qualifications

Graduate or diploma from a study coordinator training program is preferred.

One year of clinical research experience is preferred.