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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 Clinical Research Coordinator to fulfill an immediate vacancy in Kingwood, TX
· The Research Coordinator position is responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.
· Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”
· During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
· Performs routine operational activities for multiple research protocols
· Liaise between site research personnel, industry sponsors, and Supervisor
· Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
· Coordinates schedule of assessments from initial submission of feasibility until study closeout
· Reviews the study design and inclusion/exclusion criteria with physician and patient
· Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
· Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
· Creates study specific tools for source documentation when not provided by sponsor
· Collects, completes, and enters data into study specific case report forms or electronic data capture systems
· Generates and tracks drug shipments, device shipments, and supplies as needed
· Ensures timely and accurate data completion
· Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
· Communicates all protocol-related issues to appropriate study personnel or manager
· Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required
· Reviews and responds to any monitoring and auditing findings
We are actively speaking with applicants that have a minimum of:
· Must have at least 3 years of clinical research coordinator 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 - TX
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 Clinical Research Coordinator to fulfill an immediate vacancy in Kingwood, TX
· The Research Coordinator position is responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.
· Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”
· During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
· Performs routine operational activities for multiple research protocols
· Liaise between site research personnel, industry sponsors, and Supervisor
· Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
· Coordinates schedule of assessments from initial submission of feasibility until study closeout
· Reviews the study design and inclusion/exclusion criteria with physician and patient
· Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
· Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
· Creates study specific tools for source documentation when not provided by sponsor
· Collects, completes, and enters data into study specific case report forms or electronic data capture systems
· Generates and tracks drug shipments, device shipments, and supplies as needed
· Ensures timely and accurate data completion
· Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
· Communicates all protocol-related issues to appropriate study personnel or manager
· Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required
· Reviews and responds to any monitoring and auditing findings
We are actively speaking with applicants that have a minimum of:
· Must have at least 3 years of clinical research coordinator 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 and around Kingwood, Texas! Nestled in the heart of the Lone Star State, Kingwood offers a unique blend of vibrant community life, excellent schools, and abundant recreational opportunities. Known for its lush greenery and scenic beauty, this area boasts close proximity to Lake Houston for water activities and has a variety of parks and trails for outdoor enthusiasts. With renowned cultural attractions like the Kingwood Center for the Performing Arts and local eateries serving up delicious Texan cuisine, working in Kingwood promises not only a fulfilling career but also a rich and inviting lifestyle. Explore our job listings today and unlock your potential in this charming region!
