Assistant Clinical Research Coordinator II

ALLIANCE CLINICAL LLC; Dallas (TX); On-site; USD 60,000 - 90,000; Full time

Job summary

Alliance Clinical Network in Dallas, TX, seeks an Assistant Clinical Research Coordinator II to support daily clinical research operations under supervision. The role involves recruiting and enrolling participants, collecting medical history, coordinating lab tests, and maintaining study data.

The ideal candidate holds a Certified Medical Assistant credential, has 2+ years in clinical research, and is proficient with EDC systems and MS Office. Familiarity with EKGs and phlebotomy is preferred.

Qualifications

• Completion of an accredited healthcare certification program.
• Excellent verbal and written communication skills.
• Experience with clinical research concepts and documentation.

Responsibilities

• Support daily clinical research operations under supervision.
• Recruit, enroll, and retain study participants per protocol.
• Obtain and document patient medical history and concomitant medications.
• Coordinate with laboratories for timely testing and data entry into EDC systems.
• Assist with study start-up documentation, training, and timelines.

Skills

Communication skills

Attention to detail

Multitasking

Microsoft Office

Education

Certified Medical Assistant

Tools

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Assistant Clinical Research Coordinator II

FullTime Alliance Clinical Dallas, Dallas, TX, US

7 days ago Requisition ID: 1329

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.

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.
• 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.

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.