Clinical Research Monitor

Company Description M3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest...

The Clinical Research Coordinator I (CRC-I) will provide dedicated research support for clinical trials focused on complex respiratory illness (e.g., allergy, asthma, COPD, and cystic fibrosis). The CRC-I will conduct all manner of assessments relate Clinical Research, Research Coordinator, Clinical, Research, Coordinator, Monitoring, Healthcare, Education

 Are you a BC Gastroenterologist with experience in clinical trials looking to work part-time as a Sub-Investigator? M3 Wake Research has an opportunity for you in Tucson, AZ. Investigator role overview:6 hours a weekOn site presence required weeklyMust be board certified in GastroenterologyMust have experience with Sponsor Initiated Trials for...

 Are you a BC Gastroenterologist with experience in clinical trials looking to work part-time as a Sub-Investigator? M3 Wake Research has an opportunity for you in Tucson, AZ. Investigator role overview:6 hours a weekOn site presence required weeklyMust be board certified in GastroenterologyMust have experience with Sponsor Initiated Trials for...

Assist in the design and implementation of clinical research studies as directed by the EMS Division Chief. Manage EMS grants and contracts.Plan and direct the work of three (3) EMS research staff members. Manage and oversee Clinical Trial patient screening, enrollment, and follow-up. Manage and oversee data entry. Provide guidance to research faculty and...

Clinical Research Coordinator Job CategoryProfessional ScheduleFull time Shift1 - Day Shift SUMMARY: Oversees, coordinates, develops, and manages the day-to-day clinical activities for specified research trials in accordance with the research parameters established by the Principle Investigator (PI). The Clinical Research Coordinator (CRC) promotes good...

Recruit for multiple clinical trial research studies, screen/interview prospective research participants; obtain informed consent from study participants; collecting, entering, and analyzing subject data; and compiling reports. Complete/prepare approved source documentation, reports, and other materials, maintain appropriate logs, track participants, file...

The Sarver Heart Center invites applicants to apply for a Clinical Research Coordinator I position to assist in the coordination of clinical research projects by screening, interviewing, recruiting, and performing study visits. This will require comm Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Healthcare, Education, Medical

The Department of Emergency Medicine, Division of Emergency Medicine Services (EMS) is seeking a qualified individual to fill a Clinical Research Manager I position. This position will be responsible for managing ongoing research projects as well as Clinical Research, Manager, Clinical, Research, Medical Director, Compensation, Healthcare

The Division of Pulmonary, Allergy, Critical Care, and Sleep medicine, in the Department of Medicine, is seeking a candidate to lead project coordination and research participant recruitment for the University of Arizona's Community Engagement Allian Clinical Research, Research Coordinator, Clinical, Coordinator, Research, Compensation, Healthcare

  Are you a BC Gastroenterologist with experience in clinical trials looking to work part-time as a Sub-Investigator? M3 Wake Research has an opportunity for you in Tucson, AZ.  Investigator role overview: 6 hours a week On site presence required weekly Must be board certified in Gastroenterology Must have experience with Sponsor Initiated Trials for...

Screen, interview, and recruit human subjects for the Community Engagement Alliance (CEAL) research project ensuring eligibility requirements are met and patients have a complete understanding of the informed consent process.Utilize expert written and oral communication skills to provide instruction to student and community volunteers about their roles...

The Asthma & Airway Disease Research Center invites applications for the position of Clinical Research Coordinator II. The CRC II will perform tasks surrounding clinical trials requiring some autonomy in the performance of clinical research but will Clinical Research, Research Coordinator, Clinical, Research, Coordinator, Compensation, Healthcare

The University of Arizona Health Sciences (UAHS) Clinical and Translational Sciences Research Center (CATS) is looking for a Clinical Research Coordinator I to work closely with colleagues in a fast-paced environment. This position will offer ample o Clinical Research, Research Coordinator, Clinical, Research, Coordinator, Compensation, Healthcare, Education

Company Description M3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest...

Following detailed instructions by the supervisor, assist with promoting/recruiting research participants for long-term clinical trials.Participate in routine recruitment, screening, and enrollment of study participants who meet research eligibility criteria.Help obtain consent forms for approval by Human Subjects Panel. Maintain and update recruitment and...

Work with PIs, under moderate guidance, in coordinating activities related to recruitment for clinical trials including recruitment of study participants, conduct interviews, evaluate potential participants, obtain informed consent, collect and maintain subject data, and perform research subjects' assessment and Neurologic Rating Scales (NIHSS, mRS,...

Research Coordination: Duties will include performing protocol specific procedures, including lab draws, coordinate with hospital departments for the scheduling of procedures, prep for research visits, instruct participants concerning protocol responsibilities and obtain consent signature. Develop and maintain source documentation, ensure accurate and timely...

Screen, recruit, and enroll participants for medical studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.Evaluate potential study participants to ensure they meet eligibility requirements, instruct study participants concerning research protocol, and complete the patient informed...

Research Development, Design and Execution: Develops, plans, designs, and conducts research.Reviews progress and evaluates results forwarding the generation of new knowledge and understanding surrounding the impact of biological and mechanical activation of whole blood and blood platelets related to thrombotic events specifically targeting the bleeding and...