The Department of Dermatology seeks an experienced Clinical Research Coordinator II to support the clinical research of Dr. Beth Drolet and Dr. Bridget Shields. This position will join our team of world-renowned researchers and investigators committed to basic clinical and translational research designed to address dermatologic diseases and other skin-related research questions. The successful candidate will play a pivotal role in contributing to the conduct of state-of-the-art skin disease research to advance scientific knowledge and thus provide better care to patients.
Responsibilities Include:
Protocol Development and Management: Collaborate on research protocols and ensure compliance.
Regulatory Compliance and Ethics Oversight: Ensure adherence to regulations and ethical standards.
Participant Recruitment and Consent Management: Strategize recruitment strategies and manage informed consent processes.
Data Oversight and Quality Control: Oversee data collection verification and maintain quality control.
Site Coordination and Monitoring: Coordinate site activities conduct monitoring visits and ensure safety.
Communication and Reporting: Serve as the main contact communicate study progress and generate reports.
This position may require some work to be performed in-person onsite at a designated campus work location. Some work may be performed remotely at an offsite non-campus work location.
Candidates who demonstrate the following knowledge skills and abilities will be given first consideration.
Strong oral and written communication skills.
Ability to interact well with patients and researchers independently facilitating problem-solving in difficult situations.
Strong attention to detail.
Ability to use good initiative and judgement.
Ability to structure time to meet multiple deadlines.
Proficiency with Word Excel PowerPoint Outlook scheduling and project management tools such as Smartsheet.
Collaborates with departmental and institutional clinical research teams and resources performing administrative duties such as clinical research finance needs and assisting with training of staff to support study conduct and compliance
Manages regulatory and compliance activities including preparing and submitting protocols and amendments to Institutional Review Boards (IRBs) coordinating and executing Data Transfer Agreements (DTAs) and Material Transfer Agreements (MTAs) and ensuring all study activities comply with institutional federal and sponsor requirements
School of Medicine and Public Health Department of Dermatology Clinical Research Administration.
The Department of Dermatology is committed to advancing cutting-edge research training the next generation of leaders and delivering world-class patient care for individuals of all ages. Guided by our vision to be a world leader in academic dermatology we strive to be a center for remarkable care and a vibrant community dedicated to innovation education and inclusion. We embrace both independent and collaborative approaches to our work. Our philosophy is to empower individuals through comprehensive hands-on training and onboarding while fostering a strong team culture through regular collaboration with colleagues and support staff across the department.
The starting salary for the position is $54120 but is negotiable based on experience and qualifications.
Employees in this position can expect to receive benefits such as generous vacation holidays and sick leave; competitive insurances and savings accounts; retirement benefits. For more information refer to the campus benefits webpage.
1-2 years working in a research or clinical research or clinical trials environment required.
Experience in project management including the ability to manage several projects at one time
Experience working with people from varying professions and backgrounds including collaborators participants and families
Experience with clinical research regulations including OHRP CTMS GCP preferred
Demonstrated experience in scheduling coordinating and conducting visits and study meetings preferred
Experience in approaching patients to discuss clinical trials and their potential participation and obtaining informed consent preferred.
Bachelors Degree Preferred.
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Beth Reuter ejreuter@
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