Senior Clinical Research Coordinator

Clinical Research Coordinator-Onsite Job Description Clinical Research Coordinator will oversee all aspects of study execution, with a strong focus on Phase 1 and Phase 1b operations, including phlebotomy, EKGs, specimen handling, and patient visit coordination. This position is ideal for a Licensed Practical Nurse, Registered Nurse, or seasoned Clinical Research Coordinator who thrives in a highly structured, protocol-driven environment and is ready to play a key role in restarting enrollment at a dedicated research site. Responsibilities * Manage all aspects of study execution for a Phase 1b Atopic Dermatitis clinical trial involving oral investigational medication. * Coordinate and conduct ACUP2 dosing visits in strict accordance with the study protocol. * Schedule and oversee Visit 1 on Mondays and Visit 5 on Fridays, ensuring adherence to protocol requirements and participant availability. * Support and manage approximately 10-hour study days for Visits 1 and 5, including participant flow, assessments, and documentation. * Perform hands-on phlebotomy, including blood draws, sample labeling, and proper handling according to study and laboratory guidelines. * Conduct EKGs, ensuring accurate acquisition, documentation, and timely reporting of results. * Handle specimen processing, including centrifugation, aliquoting, storage, and shipment, following protocol and regulatory requirements. * Perform breathalyzer testing as required by the study protocol and document results accurately. * Maintain complete, accurate, and timely source documentation and case report forms for all study visits and procedures. * Ensure protocol compliance at all times, identifying and resolving issues that could impact data quality or participant safety. * Coordinate closely with the Sub-Investigator, remote Regulatory Coordinator, and onsite CRC to ensure seamless study operations. * Communicate with participants to explain study procedures, visit schedules, and expectations, ensuring a positive and informed participant experience. * Monitor participants during long visit days for safety, comfort, and adherence to study requirements. * Assist with the start-up and execution of additional studies as they come online, leveraging Phase 1 experience to support new protocols. * Collaborate with the broader research team to maintain high standards of Good Clinical Practice and regulatory compliance. * Support site readiness by helping maintain study supplies, equipment, and documentation in an audit-ready state. Essential Skills * Several years of clinical research experience, with a preference for candidates with multiple years in a coordinator or nursing role. * Prior Phase 1 clinical research experience, with Phase 1b exposure strongly preferred. * Hands-on phlebotomy experience, including confident and independent blood draw skills. * Experience performing EKGs in a clinical or research setting. * Proficiency in specimen processing and handling, including preparation for laboratory analysis and shipment. * Ability to conduct breathalyzer testing and accurately document results. * Experience as a Licensed Practical Nurse (LPN), Registered Nurse (RN), or experienced Clinical Research Coordinator (CRC). * Strong understanding of clinical research protocols, including visit schedules, dosing requirements, and safety monitoring. * Ability to manage long study days (approximately 10 hours) and maintain attention to detail throughout extended visits. * Strong organizational and time management skills to coordinate multiple visits, procedures, and documentation requirements. * Effective communication skills to interact with participants and collaborate with the research team. * Capability to work independently while also functioning as part of a small, collaborative study team. Additional Skills & Qualifications * Bilingual Spanish-speaking ability is highly preferred to better support a diverse participant population. * Experience with dermatology or Atopic Dermatitis studies is beneficial, though therapeutic area experience is less critical than Phase 1 expertise. * Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements for clinical trials. * Comfort working in a fast-paced research environment where new studies may be added over time. * Residence within a reasonable commuting distance of the site, with a preference for candidates in or near Coachella Valley, Riverside, or Redlands. * Willingness and ability to start in the role as soon as possible to support the immediate restart of study enrollment. Job Type & Location This is a Contract position based out of Palm Springs, CA. Pay and Benefits The pay range for this position is $35.00 - $40.00/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: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Palm Springs,CA. Application Deadline This position is anticipated to close on Jul 28, 2026. 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. 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 View email address on click.appcast.io for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.