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Rezult Group
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Rezult Group continues to make great strides toward enhancing patient care through technology services nationwide. We are consistently looking for qualified professionals to join us in achieving success. Currently we are searching for a Senior Clinical Research Coordinator to fulfill an immediate vacancy in Manchester, NH.
· 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.
· 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
We are actively speaking with applicants that have a minimum of:
· Must have at least 3 years of clinical research experience
· Must have at least 1 year of clinical trials experience
· Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel
· 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
· Certified Clinical Research Coordinator (ACRP or CCRP) preferred
If your background, skills, and interest match the following; please apply online to ensure your credentials are reviewed by a skilled recruiter immediately. We look forward to working with you on this opportunity. For more information on Rezult Group and a list of additional job openings, please visit our website at www.rezultgroup.com.
Clinical Research Coordinator - NH
Job Description
Rezult Group continues to make great strides toward enhancing patient care through technology services nationwide. We are consistently looking for qualified professionals to join us in achieving success. Currently we are searching for a Senior Clinical Research Coordinator to fulfill an immediate vacancy in Manchester, NH.
· 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.
· 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
We are actively speaking with applicants that have a minimum of:
· Must have at least 3 years of clinical research experience
· Must have at least 1 year of clinical trials experience
· Computer skills with demonstrated abilities using web-based applications, electronic data capture, and MS Word or Excel
· 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
· Certified Clinical Research Coordinator (ACRP or CCRP) preferred
If your background, skills, and interest match the following; please apply online to ensure your credentials are reviewed by a skilled recruiter immediately. We look forward to working with you on this opportunity. For more information on Rezult Group and a list of additional job openings, please visit our website at www.rezultgroup.com.
Meet Your Recruiter
Brittney Schelich
Brittney Schelich is a Senior Healthcare Recruiting Partner at Rezult Group, Inc., where she specializes in connecting healthcare professionals with opportunities that align with their career goals. Her expertise in healthcare recruitment enables her to effectively identify and place top talent within the industry.
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Discover exciting job opportunities in the vibrant Manchester, New Hampshire area! Nestled in the heart of the Granite State, Manchester boasts a thriving job market with plenty of room for career advancement and personal growth. With its picturesque Merrimack River, historic landmarks like the Palace Theatre, Currier Museum of Art, and the Fisher Cats playing at Northeast Delta Dental Stadium, this city offers a unique blend of culture and charm. Explore the local culinary scene, beautiful parks like Livingston Park and McIntyre Ski Area, and take in the breathtaking scenery of nearby Lake Massabesic. Start your career journey in Manchester, NH, and unlock a world of endless possibilities!
