Actalent
Oncology Clinical Research Coordinator
We are seeking a dedicated Clinical Research Coordinator with 12 years of prior research coordination experience. The ideal candidate will have taken full responsibility in previous roles, not merely as a research assistant or backup coordinator. This role involves frequent use of EPIC and focuses on cardiovascular research. You will play a key role in managing industry-sponsored trials and regulatory tasks. Responsibilities
Coordinate and manage clinical research trials in cardiology and oncology. Handle regulatory tasks, including IRB submissions. Engage in sponsor correspondence, excluding budget and contracting. Conduct the informed consent process with participants. Schedule standard-of-care procedures. Ensure investigational product accountability. Collaborate with local nurses for blood draws. Maintain direct communication with investigators and actively manage client engagement. Pre-screen patients and handle recruitment processes. Perform data entry and utilize electronic data capture (EDC) systems. Essential Skills
12 years of experience in clinical research coordination. Proficiency in using EPIC. Experience in oncology coordination, particularly in leading trials for 2-3+ years. Strong understanding of GCP and IRB regulations. Effective communication and organizational skills. Additional Skills & Qualifications
Prior cardiovascular experience or relevant education supporting cardiology terminology. Bilingual candidates are preferred, although translation services are available. Familiarity with Informed Consent Forms (ICF) and interpreter coordination. Job Type & Location
This is a Contract position based out of Tacoma, Washington. Pay and Benefits
The pay range for this position is $35.00 - $39.00/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 Tacoma,WA. Application Deadline
This position is anticipated to close on Aug 22, 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. 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 due to a disability, please email actALENTaccommodation@actalentservices.com for other accommodation options.
We are seeking a dedicated Clinical Research Coordinator with 12 years of prior research coordination experience. The ideal candidate will have taken full responsibility in previous roles, not merely as a research assistant or backup coordinator. This role involves frequent use of EPIC and focuses on cardiovascular research. You will play a key role in managing industry-sponsored trials and regulatory tasks. Responsibilities
Coordinate and manage clinical research trials in cardiology and oncology. Handle regulatory tasks, including IRB submissions. Engage in sponsor correspondence, excluding budget and contracting. Conduct the informed consent process with participants. Schedule standard-of-care procedures. Ensure investigational product accountability. Collaborate with local nurses for blood draws. Maintain direct communication with investigators and actively manage client engagement. Pre-screen patients and handle recruitment processes. Perform data entry and utilize electronic data capture (EDC) systems. Essential Skills
12 years of experience in clinical research coordination. Proficiency in using EPIC. Experience in oncology coordination, particularly in leading trials for 2-3+ years. Strong understanding of GCP and IRB regulations. Effective communication and organizational skills. Additional Skills & Qualifications
Prior cardiovascular experience or relevant education supporting cardiology terminology. Bilingual candidates are preferred, although translation services are available. Familiarity with Informed Consent Forms (ICF) and interpreter coordination. Job Type & Location
This is a Contract position based out of Tacoma, Washington. Pay and Benefits
The pay range for this position is $35.00 - $39.00/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 Tacoma,WA. Application Deadline
This position is anticipated to close on Aug 22, 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. 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 due to a disability, please email actALENTaccommodation@actalentservices.com for other accommodation options.