Clinical Research Coordinator - Contract - Wichita, KS
Proclinical is seeking a Clinical Research Coordinator to support the management and execution of clinical trials in the diabetes therapy area. This position also involves mentoring junior team members and addressing challenges that arise during the course of clinical studies.
Primary Responsibilities:
The successful candidate will oversee daily trial operations, ensure regulatory compliance, and collaborate with various stakeholders, including study sponsors, monitors, and site management.
Skills & Requirements:
- Clinical research experience, including familiarity with regulatory compliance and study protocols.
- Proficiency in phlebotomy and handling laboratory specimens.
- Strong organizational skills and attention to detail for managing study documentation and timelines.
- Effective communication skills for interacting with patients, caregivers, and study stakeholders.
- Ability to mentor and guide junior team members on standard operating procedures (SOPs).
The Clinical Research Coordinator's responsibilities will be:
- Manage the enrollment process for clinical trials, aiming to exceed recruitment goals.
- Collaborate with recruitment teams and site management to optimize patient recruitment strategies.
- Educate patients and caregivers about study protocols and procedures.
- Monitor study activities to ensure adherence to protocols and regulatory requirements.
- Maintain and self-audit e-regulatory binders, ensuring all documentation is up-to-date and compliant.
- Schedule study visits and monitor timelines according to protocol requirements.
- Collect and document source data during patient visits, ensuring accuracy and completeness.
- Enter collected data into electronic data capture (EDC) systems within one business day and resolve queries within 48 hours.
- Manage inventory of lab and study supplies to meet study needs and enrollment goals.
- Attend investigator meetings and site initiation visits, gathering relevant study information.
- Maintain accurate records of study activities, including case report forms and drug dispensation logs.
- Perform protocol-specific procedures such as vital signs, electrocardiograms, and specimen collection.
- Record and report adverse events, collaborating with investigators as needed.
- Oversee investigational product (IP) management, including storage, labeling, and accountability.
- Participate in quality assurance audits and ensure compliance with safety reporting requirements.
- Maintain confidentiality of patient health information and sponsor data.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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