Job description

Clinical Research Coordinator 2023Healthy MindSet Intl, Inc., DBA Diabetes & Endocrine Treatment Specialists, is seeking a Clinical Research Coordinator to manage and coordinate the timely handling of all components of clinical research protocols.

Do you want to work with a world-class Endocrinology Clinic and growing Clinical Research Site? Are you someone who excels in a cross-functional, team-oriented role? Are you a multi-tasker who demonstrates personal accountability? Are you an entrepreneurial thinker committed to advancing new medical devices or medicine? Would you provide first-in-class service to our patients who would join us in clinical research? Then keep reading. This job might be what you are looking for.

This position includes pre and post-research activities, internal and external to the clinical setting. The Clinical Research Coordinator is responsible for implementing and conducting multiple research projects throughout the year. You will coordinate comprehensive patient protocol treatment schedules to maintain compliance with protocol requirements.Additionally, the Clinical Research Coordinator develops and implements effective patient recruitment strategies. They also oversee and participate in subject recruitment, screening, scheduling, testing, and data management for multi-faceted investigations.As a result of the hard-working nature of the Clinical Research Coordinator we are looking for, you will do a little bit of everything through cross-training. You will be proficient in our EHR systems and have a solid administrative skill set. You excel at customer service, and patient care is second nature. Our Clinical Research Coordinator is flexible, driven, and excited to learn about anything and everything each study has to offer.

Duties & Responsibilities

Execute informed consent process and monitors patient status; Enroll participants into programs. Explain the research protocols to the patients and supporting family/friends, and obtain appropriate consent forms.

Assist in establishing and coordinating the implementation of clinical research protocol priorities and organization structure.

Notify and inform PIs, physicians, clinical staff, and sponsors of adverse events and protocol modifications, including their impact on the clinical research program.

Coordinate the activation and maintenance of clinical protocols, including reviewing and completing submissions, amendments, and adverse event reports as required.

Review laboratory and clinical procedures and evaluations regularly to ensure protocol compliance. Communicate clinical information and work with stakeholders to create best practice tools.

Assist physicians and clinical staff in patient identification, recruitment, and enrollment strategies to increase enrollment and meet clinical research protocols.
Analyze retention rates and formulates plans to retain participants.

Coordinate outreach to and liaison with staff at referring clinics and current patients to recruit new participants if needed.

Execute informed consent process and monitors patient status; Enroll participants into programs; explain the research protocols to the clients and supporting family/friends; and obtain appropriate consent forms.

Ensure that participant enrollment and research activities comply with established protocols, regulatory and monitoring agency standards, and sponsor guidelines.

Participate in conducting surveys of participants and supporting family/friends.
Collect and review client evaluations/assessments, surveys, and participant interviews to develop reports for the PI, appropriate agencies, and grant sponsors.

Evaluate data to determine project effectiveness.

Assist investigators in preparing study data, literature reviews, and analysis for meeting presentations and publications.

Perform other related duties and participate in special projects as assigned.

Minimum Qualifications

Bachelor’s degree in nursing or a related field is required.

At least one year of experience in coordinating a clinical research trial required
Knowledge of research protocols, principles, and procedures; knowledge of aspects of clinical trials such as screening, interviewing, and case report forms; knowledge of experimental design, mathematics, statistics, computer applications, and computer data management.

Strong verbal and written communication skills.

Preferred Qualifications

A certified Clinical Research Coordinator (CCRC) preferred
Understanding of Diabetes and Endocrine

Ready to be part of something bigger than yourself? We are excited to review your resume and cover letter explaining why you would be a good fit for our unique and fun team.Please include an email address where we can best reach you in your resume, as that is our first point of contact for applicants.

Diabetes & Endocrine Treatment Specialists is an equal opportunity employer, including but not limited to disability and/or veteran status, and complies with all applicable state and federal employment mandates. Please visit Required Employment Notices and Posters to view our non-discrimination statement and find additional information about required background checks, sexual harassment/misconduct disclosures, COVID-19 vaccination requirements, and employment eligibility review through E-Verify.

Employment Type
Full-time

Job Type: Full-time

Pay: $21.00 - $27.50 per hour

Benefits:

• Dental insurance
• Employee discount
• Flexible schedule
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Professional development assistance
• Tuition reimbursement
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday
• No nights
• No weekends

Ability to commute/relocate:

• Sandy, UT 84093: Reliably commute or planning to relocate before starting work (Required)

Work Location: In person

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