Clinical Research Coordinator I

Alliance Clinical Network; Houston (TX); Vor Ort; USD 52.000 - 76.000; Vollzeit

Zusammenfassung

Alliance Clinical Network seeks a Clinical Research Coordinator I to support clinical trials by coordinating visits, collecting data, and ensuring protocol and regulatory compliance. The CRC will interact with participants, monitor health, and collaborate with the PI to uphold Good Clinical Practice (GCP) standards.

The role includes EKGs, data entry into EDC systems, and coordination with laboratories to ensure timely testing and reporting, while maintaining strict confidentiality and

Qualifikationen

• 2 years of phlebotomy and EKG procedures; CPT license preferred.
• Associate’s degree in healthcare or related field, or equivalent experience.
• Minimum 2 years of healthcare experience.
• Minimum 2 years of FDA regulations and Good Clinical Practice (GCP).
• Demonstrated analytical reasoning skills.
• Exceptional attention to detail and strong organizational skills.
• Excellent verbal and written communication abilities.
• Proven customer service skills with internal and external stakeholders.
• Ability to effectively manage multiple priorities in a fast-paced environment.

Aufgaben

• Coordinate study visits and data collection.
• Monitor participant health throughout the trial.
• Obtain informed consent and document patient history.
• Maintain regulatory files and ensure protocol compliance.
• Enter data into EDC and resolve data queries.
• Assist with monitoring visits and site readiness.

Kenntnisse

Phlebotomy

EKG

Analytical reasoning

Attention to detail

Organizational skills

Verbal communication

Written communication

Customer service

Multitasking

Ausbildung

Associate’s degree in healthcare or related field

Jobbeschreibung

Summary

The Clinical Research Coordinator I (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants including monitoring the health of each participant throughout the trial. The CRC plays a key part in maintaining study integrity and quality and collaborating with the Principal Investigator (PI) to provide oversight of the study to ensure adherence to Good Clinical Practice (GCP) guidelines.

• Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
• Adhere to site standard operating procedures (SOPs).
• Administer questionnaires and monitor participant compliance with study protocols.
• Respond to participant needs promptly and appropriately.
• Collect and document patient medical history and health conditions.
• Obtain and document informed consent from study participants.
• Maintain accurate records of investigational product (IP) dispensation and accountability.
• Coordinate with laboratories to ensure timely testing and reporting.
• Collect and document information on concomitant medications.
• Review medical records for protocol compliance.
• Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).
• Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
• Review clinical laboratory reports in accordance with protocol requirements.
• Maintain up-to-date regulatory files for the research site.
• Verify the accuracy and completeness of collected data.
• Monitor and document temperatures for IP storage.
• Support recruitment and engagement of study participants as needed.
• Develop electronic source (eSource) documents in accordance with study protocols.
• Manage study startup documentation, training, and timelines for assigned protocols.
• Ensure all protocol requirements and deadlines are met consistently.
• Maintain strict confidentiality and compliance with regulatory standards.
• Assist with preparation for monitoring visits.
• Enter data into electronic data capture (EDC) systems and resolve data queries.
• Perform other duties as assigned.

Summary

The Clinical Research Coordinator I (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction with participants including monitoring the health of each participant throughout the trial. The CRC plays a key part in maintaining study integrity and quality and collaborating with the Principal Investigator (PI) to provide oversight of the study to ensure adherence to Good Clinical Practice (GCP) guidelines.

Essential Duties And Responsibilities

• Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
• Adhere to site standard operating procedures (SOPs).
• Administer questionnaires and monitor participant compliance with study protocols.
• Respond to participant needs promptly and appropriately.
• Collect and document patient medical history and health conditions.
• Obtain and document informed consent from study participants.
• Maintain accurate records of investigational product (IP) dispensation and accountability.
• Coordinate with laboratories to ensure timely testing and reporting.
• Collect and document information on concomitant medications.
• Review medical records for protocol compliance.
• Perform and document assessments for adverse events (AEs) and serious adverse events (SAEs).
• Conduct clinical procedures including EKGs, vital signs, nasal swabs, and other protocol-specific tasks.
• Review clinical laboratory reports in accordance with protocol requirements.
• Maintain up-to-date regulatory files for the research site.
• Verify the accuracy and completeness of collected data.
• Monitor and document temperatures for IP storage.
• Support recruitment and engagement of study participants as needed.
• Develop electronic source (eSource) documents in accordance with study protocols.
• Manage study startup documentation, training, and timelines for assigned protocols.
• Ensure all protocol requirements and deadlines are met consistently.
• Maintain strict confidentiality and compliance with regulatory standards.
• Assist with preparation for monitoring visits.
• Enter data into electronic data capture (EDC) systems and resolve data queries.
• Perform other duties as assigned.

Qualifications

• 2 years of experience with phlebotomy and EKG procedures, with a current Certified Phlebotomy Technician (CPT) license preferred.
• Associate’s degree in healthcare or a related field, or equivalent relevant experience.
• Minimum of 2 years of experience in a healthcare setting.
• Minimum of 2 years of experience with FDA regulations and Good Clinical Practice (GCP).
• Demonstrated analytical reasoning skills.
• Exceptional attention to detail and strong organizational skills.
• Excellent verbal and written communication abilities.
• Proven customer service skills with both internal and external stakeholders.
• Ability to effectively manage multiple priorities in a fast-paced environment.

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.

About The Company

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.