Clinical Research Coordinator

Description Will be working on dermatology industry-initiated clinical trials Usally assign studies by sponsor 11-15 studies per coordinator Will see 20-25 patients per week Enrollment: Dr. works at the clinic and handles 95% of the recruitment from the clinic side; they do not struggle to meet enrollment The Clinical Research Coordinator leads and manages clinical trials in compliance with regulatory standards, working closely with the investigative team, pharmaceutical sponsors, and research participants. This role requires a strong medical experience, proficiency in Good Clinical Practices (GCP), FDA regulations, and a commitment to ethical research standards. KEY RESPONSIBILITIES: Duties will include, but are not limited to: u2022 Manage and oversee the execution of clinical trials under the direction of the Principal Investigator and Site Manager. u2022 Conduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring. u2022 Administer questionnaires, diaries, and other participant materials as per protocol. u2022 Schedule and coordinate research visits, assessments, and procedures, ensuring all requirements are met. u2022 Maintain accurate case report forms, cross-referencing patient medical records for completeness and FDA compliance. u2022 Collect, enter, and manage clinical data while maintaining confidentiality. u2022 Monitor study participants, ensuring adherence to study guidelines and ethical standards. u2022 Manage investigational medications, including receiving, dispensing, and performing drug accountability. u2022 Collaborate with laboratories to process, ship, and ensure review of investigational reports. u2022 Actively participate in recruiting and screening study participants. u2022 Maintain organized records of study materials, ensuring all regulatory documentation is up to date. u2022 Ensure necessary supplies and equipment are available and functional for each study. u2022 Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services. EDUCATION REQUIREMENTS: u2022 High School Diploma or GED u2022 Preferred: Bacheloru2019s or Masteru2019s degree in a related field. EXPERIENCE: u2022 Required: Previous experience conducting clinical trials, including recruitment and compliance with regulatory guidelines. u2022 Preferred: Certification as a Clinical Research Coordinator (CCRC). Job Type & Location This is a Contract position based out of Fountain Valley, CA. Pay and Benefits The pay range for this position is $28.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Fountain Valley,CA. Application Deadline This position is anticipated to close on Apr 3, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is 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 Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, weu2019ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APACu2014with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at .

Created: 2026-03-30