Job Title: Clinical Research Coordinator

Job Description

Provide clinical research support to investigators to prepare for and execute assigned research studies. Responsibilities include data collection, maintaining research subject study data, recruiting and screening participants, and ensuring compliance with regulatory and ethical guidelines.

Responsibilities

• Collect, record, and maintain research subject study data according to study protocols and SOPs, ensuring quality control for content, accuracy, and completeness.
• Collect and submit regulatory/ethics documentation as required by regulatory bodies governing clinical research.
• Recruit and screen participants for clinical trials and maintain subject screening logs.
• Assist in the consent process and orient research subjects to the study.
• Maintain source documentation based on protocol requirements.
• Schedule and execute study visits and perform study procedures.
• Handle lab testing and analysis, including specimen collection, shipment, and logistics.
• Monitor subject safety and report adverse events to the Principal Investigator or medical personnel.
• Correspond with research subjects to troubleshoot study-related questions or issues.
• Participate in team huddles to confirm daily study tasks.
• Assist with study data quality checking and query resolution.
• Perform complex clinical research procedures, including ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
• Assist investigators in meeting research study objectives on time and within budget.
• Provide training to new investigator site staff members on study-specific topics.
• Prepare for and attend study monitoring visits, audits, and regulatory inspections.
• Assist with coverage planning related to staffing and scheduling for research studies.
• Maintain confidentiality of data and PHI.
• Collaborate with provider offices to carry out research efficiently.
• Maintain stock of supplies needed for each study per protocol.
• Perform other duties and projects as assigned.

Essential Skills

• Minimum of 1-2 years on-site CRC experience.
• Proficient in Microsoft Office applications.
• Understanding of medical terminology.
• Working knowledge of clinical trials and ability to apply GCP/ICH and FDA regulations.
• In-depth knowledge of departmental, protocol, and study-specific operating procedures.
• Skilled in carrying out clinical procedures such as phlebotomy and vital signs monitoring.
• Excellent written and verbal communication skills.
• 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.
• Ability to establish and maintain effective working relationships.
• Practice a high level of integrity and confidentiality.

Additional Skills & Qualifications

• 1-2 years of clinical research experience.
• Relevant work experience in a clinical environment or medical setting.
• Drug trial experience is preferred but not required.
• Phlebotomy experience is a plus.

Work Environment

This position requires working five days on-site at the clinic. The environment involves direct patient interaction, handling lab specimens, and performing various clinical procedures. Adherence to clinic-specific protocols and maintaining confidentiality is essential.

Pay and Benefits

The pay range for this position is $48000.00 - $67000.00/yr.

Competitive salary
Health Insurance
Dental Insurance
Disability Insurance
Life Insurance
Paid Time Off
Vision Insurance

Workplace Type

This is a fully onsite position in Charlotte,NC.

Application Deadline

This position is anticipated to close on Mar 21, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $48,000 - $67,000