Clinical Research Coordinator Associate

How to Apply

A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

The cover letter should address your specific interest in the position, outline skills and experience that directly relate to this position and provide three references with full contact information (name, phone number, e-mail address). If you are not providing a reference from your current position, please explain why. Applications without a complete cover letter will not be considered.

Mission Statement Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.

Job Summary The De Lott Research Group in the Department of Ophthalmology and Visual Sciences at the University of Michigan Kellogg Eye Center is seeking a detail-oriented, highly motivated, and compassionate Clinical Research Coordinator - Associate. The coordinator will support prospective, multi-institutional clinical research studies focused on chronic ocular pain and other neuro-ophthalmic conditions.

This position will work closely with Principal Investigator Dr. Lindsey De Lott, another clinical research coordinator, co-investigators and research staff at collaborating institutions, and clinical partners. The coordinator will support participant recruitment and retention, study visits, regulatory and data-management activities, and the execution of established protocols and workflows. A key responsibility will be assisting the group's other coordinator with quantitative sensory testing and other portions of study visits

The successful candidate will be dependable, organized, attentive to detail, and able to manage multiple responsibilities while working independently within established procedures and collaboratively as part of a multidisciplinary team. Strong communication, follow-through, participant-centered professionalism, and the ability to identify and escalate issues appropriately are essential.

We value different perspectives and are committed to fostering a collaborative environment in which every team member can thrive and contribute to our collective success.

CRC Statement This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies depending on complexity that range from moderate to complex. Coordinator experience and mastery of all job duties from the CRC-Technician position on the Michigan Medicine CRC Career Ladder is required. This position should be able to perform tasks and make decisions independently, consistently, and accurately, and demonstrate that they have achieved a moderate level of expertise in all their skills and abilities resulting in high quality work.

It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies, navigate available resources appropriately, effectively use all tools and job aids at their disposal and operate e-clinical technologies with a reasonable degree of proficiency. This position can perform the majority of tasks independently and perform quality checks of their work.

They also know where and how to identify appropriate resources and support and are able to discern when to escalate issues needing additional intervention. Key behavioral competency descriptors include demonstrate, implement, execute, and use.

Responsibilities
* Independent knowledge, skills, and abilities within all eight competency domains are expected:

Scientific Concepts and Research Design Ethical Participant Safety Considerations Investigational Products Development and Regulation Clinical Study Operations and Good Clinical Practice Study and Site Management Data Management and Informatics Leadership and Professionalism Communication and Teamwork Responsibilities will include, but are not limited to, the following.

Clinical Research Coordination Understand protocol elements and requirements and accurately implement study procedures.

Coordinate assigned activities for multiple…