Manage and coordinate oncology clinical research trials, including patient recruitment, protocol development, and data management.
Oversee oncology trials and research projects
Develop research protocols and grant proposals
Perform patient evaluations and administer medications
Train and supervise staff
Ensure compliance with regulations through audits
Manage financial accounts and authorize purchases
Develop strategies for participant recruitment and retention
Interface with study sponsors and resolve queries
Monitor IRB submissions and respond to requests
MUST be able to relocate on your own to the Atlanta, GA area (no relocation offered)
MUST have Clinical Research Coordinator (CRC) experience
3+ years of solid CRC experience in oncology or interventional drug trials in other therapeutic areas
Two years of college in a scientific, health related, or business administration program AND 3 years of clinical research experience
OR High School Diploma or GED AND 3+ years of clinical research experience
The pay range for this position is $28.00 - $30.00/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:
This is a fully onsite position in Charleston, SC.
This position is anticipated to close on May 2, 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.
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.
Clinical Research Coordinator (LOCATED In Atlanta) • Charleston, SC, United States
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