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Job type: Contract

Discipline: Clinical Research Associate (CRA)

Location: United States

Clinical Research Coordinator - Contract - Longmont, CO

Are you ready to drive the future of clinical research and be at the heart of a company where precision meets purpose?

��ý��ygfcmw��(�й�)վ��ֱ�ӽ� is seeking a Clinical Research Coordinator to oversee the daily operations and management of assigned clinical trials.

Primary Responsibilities:

This role involves administrative duties, regulatory compliance, and collaboration with various stakeholders, including study sponsors, monitors, CROs, principal investigators, and site management. You will also guide and train junior team members while ensuring adherence to protocols and organizational standards.

Skills & Requirements:

Clinical research experience, including familiarity with protocols and regulatory compliance.
Phlebotomy skills and experience.
Strong organizational and problem-solving abilities.
Effective communication and collaboration skills.
Proficiency in data collection and electronic data capture systems.
Ability to manage multiple tasks and prioritize effectively.

The Research Scientist's responsibilities will be:

Manage enrollment for clinical trials, identifying strategies to exceed recruitment goals.
Collaborate with recruitment teams and site management to optimize patient recruitment practices.
Inform patients or caregivers about study procedures and requirements.
Monitor study activities to ensure compliance with protocols and regulatory guidelines.
Maintain and update study e-regulatory binders, ensuring documentation accuracy and completeness.
Schedule study visits and monitor timelines according to protocol requirements.
Collect and document data during patient visits, ensuring timely entry into electronic data capture (EDC) systems.
Resolve data queries within specified timelines.
Manage inventory of lab and study supplies to meet enrollment and study visit needs.
Attend investigator meetings and site initiation visits, gathering relevant study information.
Perform protocol-specific procedures, such as vital signs, electrocardiograms, and specimen collection.
Record adverse events and collaborate with investigators on reporting requirements.
Oversee drug accountability, including logging shipments, dispensation, and compliance tracking.
Maintain accurate master logs for each study, including informed consent and enrollment records.
Participate in quality assurance audits and ensure investigational product (IP) management compliance.
Maintain training logs, delegation logs, and safety reports for assigned studies.
Ensure confidentiality of patient health information and sponsor data.

Compensation:

$22 to $26 per hour.

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.

��ý��ygfcmw��(�й�)վ��ֱ�ӽ� is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ��ý��ygfcmw��(�й�)վ��ֱ�ӽ� is acting as an Employment Agency in relation to this vacancy.

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