Clinical Research Coordinator

Job Description:

Are you a dedicated and hardworking professional with Research Coordination experience? Do you have an understanding of Medical Terminology?

Apply today to join a team where your growth, well-being, and success are our top priority!

Details:

• $35.86 per hour pay rate
• Full Time
• Contract
• Schedule: 7am - 4pm M-F
• Onsite in Kingwood, TX

What's in it for you?

• Health, Dental, Vision insurance offered
• 401k options
• Work with a great team!

Only considering candidates with the following:

• Bachelor's Degree and 1 + Years of Relevant Exp - Required
• Certified Clinical research Coordinator Preferred
• Knowledge of organizational policies, standard operating procedures, and systems
• Emerging understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment.
• Basic understanding of medical terminology
• Effective communication skills
• Strong organizational skills and time management
• Basic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping
• An underlying, enduring trait useful for performing duties
• Interpersonal skills
• Self-motivated
• Meticulous eye for detail
• Clinical Competencies: This role may require competency in performing clinical tasks, including ECG, phlebotomy, and the process of handling, centrifuging, storing and shipping of specimens. Demonstrating the ability to perform core competencies will be evaluated, at a minimum, annually. Training and/or certification will be provided when mandatory, per protocol.
• Proof of specified vaccines

Responsibilities:

• 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 Supervise
• 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

$ 35.86/hr

Prof23