Assistant Clinical Research Coordinator II

Alliance Clinical Network; Dallas (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Alliance Clinical Network in Dallas, TX is seeking an Assistant Clinical Research Coordinator II to support daily clinical research operations under supervision of the Site Manager and Principal Investigator. You will help with patient recruitment, enrollment, and retention while ensuring protocol compliance.

Key duties include coordinating with laboratories, collecting medical history and concomitant medications, administering informed consent, entering data into EDC systems, and maintaining

Qualifications

• Completion of an accredited healthcare certification program is required; approximately 2–3 years of clinical research experience.
• 2 years of experience in running research protocols preferred
• Minimum of 2 years of experience in FDA regulations and Good Clinical Practice (GCP) required.

Responsibilities

• Assist the CRC and senior team as requested to facilitate research and business needs.
• Communicate effectively and courteously with study patients regarding study objectives and ongoing instructions.
• Administer questionnaires and monitor participant compliance.
• Acknowledge study patients' needs and tend to them appropriately.
• Collect patient medical history and medical conditions.
• Obtain informed consent.
• Coordinate with laboratories to ensure timely participant testing.
• Collect and evaluate concomitant medications.
• Collect and evaluate medical records for compliance.
• Perform study procedures such as EKGs, vital signs, nasal swabs, and protocol ‑ specific procedures.
• Verify the accuracy of data collected.
• Perform administrative tasks such as ordering supplies and equipment for the study.
• Recruit patients for clinical trials based on criteria outlined in the study protocol.
• Develop study eSource documents to comply with study protocol.
• Manage all required study start-up documentation, training, and timelines on assigned study protocols.
• Meet all study protocol requirements and deadlines.
• Enter data into electronic data capture (EDC) systems and resolve data queries
• Perform other duties as assigned.

Skills

Communication skills

Attention to detail

Multitasking

Customer service

Patient interaction

Education

Healthcare certification program

Tools

Microsoft Office Suite

Job description

Summary

The Assistant Clinical Research Coordinator II (ACRC II) supports daily clinical research operations under the direction and ongoing supervision of the Site Manager, Site Director, and Principal Investigator, ensuring compliance with required protocols. Responsibilities include planning, organizing, and assisting with clinical trials by conducting patient recruitment, enrollment, and retention.

• Assist the CRC and senior team as requested to facilitate research and business needs,
• Communicate effectively and courteously with study patients regarding study objectives and ongoing instructions.
• Acknowledge study patients' needs and tend to them appropriately.
• Collect patient medical history and medical conditions.
• Coordinate with laboratories to ensure timely participant testing.
• Collect and evaluate concomitant medications.
• Collect and evaluate medical records for compliance.
• Perform study procedures such as EKGs, vital signs, nasal swabs, and protocol ‑ specific procedures.
• Verify the accuracy of data collected.
• Perform administrative tasks such as ordering supplies and equipment for the study.
• Recruit patients for clinical trials based on criteria outlined in the study protocol.
• Develop study eSource documents to comply with study protocol.
• Manage all required study start-up documentation, training, and timelines on assigned study protocols.
• Meet all study protocol requirements and deadlines.
• Enter data into electronic data capture (EDC) systems and resolve data queries
• Perform other duties as assigned.

Essential Duties And Responsibilities

• Assist the CRC and senior team as requested to facilitate research and business needs,
• Communicate effectively and courteously with study patients regarding study objectives and ongoing instructions.
• Administer questionnaires and monitor participant compliance.
• Acknowledge study patients' needs and tend to them appropriately.
• Collect patient medical history and medical conditions.
• Obtain informed consent.
• Coordinate with laboratories to ensure timely participant testing.
• Collect and evaluate concomitant medications.
• Collect and evaluate medical records for compliance.
• Perform study procedures such as EKGs, vital signs, nasal swabs, and protocol ‑ specific procedures.
• Verify the accuracy of data collected.
• Perform administrative tasks such as ordering supplies and equipment for the study.
• Recruit patients for clinical trials based on criteria outlined in the study protocol.
• Develop study eSource documents to comply with study protocol.
• Manage all required study start-up documentation, training, and timelines on assigned study protocols.
• Meet all study protocol requirements and deadlines.
• Enter data into electronic data capture (EDC) systems and resolve data queries
• Perform other duties as assigned.

Qualifications

• Completion of an accredited healthcare certification program is required; approximately 2–3 years of clinical research experience.
• 2 years of experience in running research protocols preferred
• Minimum of 2 years of experience in FDA regulations and Good Clinical Practice (GCP) required.
• Minimum of 2 years of experience in phlebotomy and EKGs required.
• Exceptional attention to detail, organization, and the ability to multitask.
• Must possess excellent verbal and written communication skills and medical terminology knowledge.
• Excellent customer service skills with internal and external stakeholders.
• A proven ability to multitask in a rapidly changing environment.
• Experience working directly with patients/participants in a clinical setting.
• Experience in Microsoft Office Suite (Excel, Word, PowerPoint).

Certificates, Licenses, And Registrations

• Certified Medical Assistant required.
• CPR/BLS certification required.
• Maintain IATA certification and other job ‑ related certifications as required.

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.