Work in Iowa Veterans Jobs

Job Title: Clinical Research Coordinator

Job Description

Provide clinical research support to investigators to prepare for and execute assigned research studies. Responsibilities include:

• Collect, record, and maintain research subject study data according to study protocols and SOPs, ensuring content, accuracy, and completeness.

• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies.

• 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 its purpose, 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 specimen collection tube preparation, 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 daily 'huddles' to confirm study tasks are assigned and executed to expected standards.

• Assist with study data quality checking and query resolution.

• Perform complex clinical research procedures such as ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.

• Assist investigators in meeting research study objectives on time, within budget, and according to applicable protocol requirements, regulations, and quality standards.

• Provide training to new site staff members on study-specific topics and maintain training records.

• 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 ensure efficient research workflow.

• Maintain stock of supplies needed for each study per protocol.

• Perform other duties and projects as assigned.

Hard Skills

• Minimum of 1 year on-site CRC experience

• Drug trial experience preferred

• Phlebotomy experience highly preferred

Soft Skills

• Attention to detail

• Strong organizational skills

• Effective communication

• Ability to troubleshoot and resolve issues

• Team collaboration

Work Environment

Site is The Iowa Clinic at West Des Moines, IA. The role requires 5 days on-site at the clinic, Monday to Friday

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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.