Senior Clinical Research Coordinator job in Manchester, NH
Manchester, NH CorTech LLC
| Job Ref: | 366399 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 44.83/Per Hour |
| Remote: | No |
Location |
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| City: | Manchester, NH |
| Post Code: | 03102 |
| Map: |
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Description |
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JobsRUs.com is seeking to hire a Senior Clinical Research Coordinator for our client in Manchester, NH! Benefits Available! Weekly Pay! 6 Month Contract Pay Rate - $44.83/hr 1st Shift: Monday-Friday, 8am-5pm, occasionally 7am Job Description The Senior Clinical Research Coordinator is responsible for coordinating multiple research protocols; serving as a liaison with local investigators and research personnel; and acting as a central resource for assigned research projects. The individual in this role offers a significant contribution to the development of processes, tools, and training necessary to maintain site compliance and patient safety. Major Responsibilities Duties include but are not limited to: · Practices and adheres to the ?Code of Conduct? philosophy and ?Mission and Value Statement? · Demonstrate ability to fulfill responsibilities and duties of the CRC Level I and II · Assist with training CRC Level I and II personnel · Act as a role model to peers Clinical Research Operations · Perform routine operational activities for multiple research protocols · Liaise between site research personnel, industry sponsors, and Supervisor · Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable · Coordinate schedule of assessments from initial submission of feasibility until study closeout · Coordinate submission and approval for the Site?s Facility Review Committee, if applicable · Provide awareness of research protocols to appropriate site-level personnel, including physicians, nurses, clinical staff, and administrators · Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.) · Accurately perform/calculate and documents the BSA, mRS, NIHSS, STS risk score, or any other approved CRC task, as needed per protocol · Document all patient, staff, and sponsor correspondence, including follow-up encounters, adverse events, interventions, pharmacy dispensations, and patient phone calls · Ensure follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements · Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP · Re-consent patients in a timely manner and document process appropriately ? Support study team in mitigating risks and optimizing site compliance Site Development · Work with site personnel and local investigators to assess site feasibility and performance · Regularly meet with physicians and administrators, when applicable, to assess study performance and investigator satisfaction · Collaborate with other departments (non-invasive, finance, laboratory, etc.) to develop and implement processes in support of the research activities · Assist with providing a research update during Site Administrative meetings (Section meetings, Site Service Line meetings, etc.) · Able to guide research team members on the management of non-compliant data and/or study activities Reporting and Analysis · Monitor patient enrollment at the site through weekly reports, and reports results to Supervisor · Facilitate continuing education and training to investigators, as applicable Required Education and Experience Bachelors degree in a related field At least one year of relevant experience Preferred Qualifications Masters degree in a related field 5+ years of relevant experience Certified Clinical Research Coordinator (ACRP or CCRP) Knowledge, Skills, and Abilities Knowledge: · Knowledge of organizational policies, standard operating procedures, and systems · Demonstrate understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment. · Fundamental understanding of medical and research operations terminology · Recognize circumstances requiring prompt escalation to PI, IRB, and/or Supervisor Skills: The proficiency to perform a certain task · Effective communication skills · Strong organizational skills and time management · Basic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping. · Effective interfacing with site stakeholders Abilities: An underlying, enduring trait useful for performing duties · Interpersonal skills · Self-motivated · Meticulous eye for detail | |
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