Clinical Research Coordinator

Kelly Science, Engineering, Technology & Telecom; Gilbert (AZ); On-site; USD 50,000 - 70,000; Full time

Job summary

A clinical research organization is looking for a Clinical Research Coordinator in Gilbert, Arizona, to support clinical studies by managing data and maintaining records. Responsibilities include recruiting participants, ensuring compliance with protocols, and monitoring subject safety. A Bachelor's degree in a related field and experience in clinical research are essential. Candidates must be proficient in Microsoft Office and possess strong communication and organizational skills.

Qualifications

• 1-2 years of clinical research experience required.
• Experience in therapeutic areas such as family medicine and diabetes preferred.
• Skilled in clinical procedures like phlebotomy.

Responsibilities

• Provide clinical research support to investigators.
• Maintain research subject study data.
• Assist in recruitment and consent processes.

Skills

Clinical research management

Data collection and analysis

Patient recruitment

Communication

Problem-solving

Time management

Education

Bachelor's degree in a related field

Tools

Microsoft Office

Job description

Join Kelly FSP as a Clinical Research Coordinator at our client site in Gilbert, Arizona.

This is a 3-6 month renewable contract opportunity.

A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; i.e., collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs, and GCPs.

Responsibilities

• Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
• Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.
• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
• Recruit and screen participants for clinical trials and maintain subject screening logs.
• Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.
• Maintain source documentation based on protocol requirements.
• Schedule and execute study visits and perform study procedures.
• Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.
• Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.
• Correspond with research subjects and troubleshoot study-related questions or issues.
• Participate in huddles to confirm daily study tasks are assigned to team members and are executed to the expected standards.
• Assist with study data quality checking and query resolution.
• Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
• Assist the investigator in verifying that research study objectives are met on time, within budget, and according to applicable protocol requirements, clinical research regulations, and quality standards.
• Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
• Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
• Assist the research site with coverage planning related to staffing and scheduling for research studies.
• Monitor subject safety and report adverse reactions to appropriate medical personnel.
• Maintain confidentiality of data and PHI as required.
• Collaborate with provider offices to carry out research in the most efficient workflow possible.
• Maintains stock of supplies needed to carry out each study per protocol.
• Performs other duties and projects as assigned.

Qualifications

• Bachelor's degree in a related field
• 1-2 years of clinical research experience
• Therapeutic areas: family medicine, type II diabetes, hypertension, some cardiac preferred
• Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience
• Proficient in the use of Microsoft Office applications
• Understanding of medical terminology
• Working knowledge of clinical trials
• Knowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device
• In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules
• Skilled in carrying out required clinical procedures such as phlebotomy and vital signs
• Strong written and verbal communication skills including good command of the English language
• Skill in applying and modifying professional research principles, methods, and techniques to provide ongoing patient care
• Skill in preparing/maintaining records, writing reports, and responding to correspondence
• Ability to maintain quality control standards
• Ability to react calmly and effectively in all situations
• Excellent organizational and problem-solving skills
• Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to detail
• Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients
• Practice a high level of integrity, honesty, and maintaining confidentiality