Arkansas Staffing
Part-Time Clinical Research Coordinator
Arkansas Staffing, Sacramento, California, United States, 95828
Job Opportunity: Clinical Research Coordinator
We are currently seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to join our team on a part-time, contract basis. This onsite role is ideal for someone with strong experience in clinical research who thrives in a collaborative yet independent work environment. The CRC will play a key role in supporting the day-to-day operations of an ongoing clinical trial, ensuring compliance with study protocols and regulatory requirements. Key Responsibilities
Study Coordination & Participant Engagement: Schedule and coordinate in-patient visits and follow-up appointments. Communicate with study participants to confirm appointments and send timely reminders. Ensure informed consent is properly obtained and documented. Data Collection & Management: Accurately collect and record study data from various sources. Enter data into electronic data capture (EDC) systems in accordance with study timelines. Maintain organized and up-to-date study documentation. Query Resolution & Compliance: Review data entries for accuracy and completeness. Respond to and resolve data queries from monitors or sponsors in a timely manner. Adhere to Good Clinical Practice (GCP) guidelines and institutional policies. Collaboration & Reporting: Work closely with investigators, study sponsors, and other research staff. Provide regular updates on study progress and any issues encountered. Assist with preparation for monitoring visits and audits. Qualifications
Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar clinical research role. Strong working knowledge of electronic medical records (EMR) and electronic data capture (EDC) systems. Excellent organizational skills and attention to detail. Ability to work independently and manage multiple tasks efficiently. Strong communication and interpersonal skills. The pay range for this position is $25.00 - $32.00/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) This is a fully onsite position in Sacramento, CA. Application deadline is anticipated to close on Aug 20, 2025. 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. 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.
We are currently seeking a dedicated and detail-oriented Clinical Research Coordinator (CRC) to join our team on a part-time, contract basis. This onsite role is ideal for someone with strong experience in clinical research who thrives in a collaborative yet independent work environment. The CRC will play a key role in supporting the day-to-day operations of an ongoing clinical trial, ensuring compliance with study protocols and regulatory requirements. Key Responsibilities
Study Coordination & Participant Engagement: Schedule and coordinate in-patient visits and follow-up appointments. Communicate with study participants to confirm appointments and send timely reminders. Ensure informed consent is properly obtained and documented. Data Collection & Management: Accurately collect and record study data from various sources. Enter data into electronic data capture (EDC) systems in accordance with study timelines. Maintain organized and up-to-date study documentation. Query Resolution & Compliance: Review data entries for accuracy and completeness. Respond to and resolve data queries from monitors or sponsors in a timely manner. Adhere to Good Clinical Practice (GCP) guidelines and institutional policies. Collaboration & Reporting: Work closely with investigators, study sponsors, and other research staff. Provide regular updates on study progress and any issues encountered. Assist with preparation for monitoring visits and audits. Qualifications
Minimum of 2 years of experience as a Clinical Research Coordinator or in a similar clinical research role. Strong working knowledge of electronic medical records (EMR) and electronic data capture (EDC) systems. Excellent organizational skills and attention to detail. Ability to work independently and manage multiple tasks efficiently. Strong communication and interpersonal skills. The pay range for this position is $25.00 - $32.00/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) This is a fully onsite position in Sacramento, CA. Application deadline is anticipated to close on Aug 20, 2025. 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. 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.