Apply for Vacancy for Clinical Research Coordinator at Indiana University in the USA. The category for this application is  Laboratory and Research.

Department Information

The Indiana University School of Medicine Department of Emergency Medicine is a statewide network of emergency departments striving to set new standards of training for medical students, residents, fellows and pre-hospital providers while providing quality care for a diverse patient population.

IU School of Medicine leads in the science of emergency medicine, operating in an environment that has rich research infrastructure, including the highest-ranked Clinical and Translational Science Institute (CTSI) in the United States and a nationally ranked medical bio-informatics institution. Multiple clinical environments present practitioners with ample opportunity to make a difference in the lives of patients on a daily basis.

Job Summary 

Under general supervision, incumbent will assist in the conduct of clinical trials and research (minimal risk) and research involving human subjects (more than minimal risk). Incumbent will perform varied routine and non-routine tasks of moderate complexity. As a Clinical Research Coordinator he/she will initiate, conduct, complete and report clinical studies. Assign and coordinate activities of study sites to ensure protocol, regulatory and standard operating procedures and Good Clinical Practices compliance. Oversee the initial training and competency of research associates including undergraduate and medical students. Able to develop solutions to complex problems that impact the timeliness and accuracy of the conduct of our clinical research. Apply for Vacancy for Research Coordinator in the USA.

Primary Duties:

• Participate in protocol review, evaluations, study design and risk assessments to subject population. Prepare, amend and submit Institutional Review Board (IRB) documents. Develop informational materials for recruitment.
• Also, identify potential subjects from review of existing protected health information based on inclusion/exclusion criteria.
• Likewise, identify, schedule screening procedures and review results. Recruit subjects and keep accurate records.
• Similarly, serve as an advocate for the subjects and their family.
• Moreover, utilize REDCAP database to create forms for physician data capture. Extract data from source documents and complete Case Report Forms (CRF) or database entries. Manage handling of laboratory specimens. Moreover, maintaining sample/specimen tracking and inventory. Prepare and present study protocol reviews at meetings.
• Also, train and orient new, less-experienced coordinators, specialist, techs, students, and volunteers; train support-personnel on study-specific tasks. Provide day to day supervision over part-time staff and students working on studies. Maintain training logs.
• Likewise, update enrollment/invoicing logs promptly for studies. Monitor enrollment goals and modify recruitment strategies as needed. Be prepared to address issues and offer solutions to increase enrollment.
• Moreover, maintain current knowledge of regulatory affairs and/or issues. Maintain a high level of expertise through familiarity of clinical literature and/or attending continuing education classes, conferences, seminars, and project team meetings.

Preferred Qualifications

Phlebotomy certification.

Working Conditions / Demands

Requires mobility between hospital sites, must be able to communicate well, use a laptop computer. Also, transport study equipment to various locations.

Work Location

Eskenazi Health Hospital and IU Health hospitals

Indianapolis, Indiana

Visit oyaop.com  for more job opportunities.