What are the responsibilities and job description for the Clinical Research Specialist position at Actalent?
CLINICAL RESEARCH SPECIALIST
Study Start-Up & Regulatory Compliance:
Facilitate study initiation, including regulatory document collection and IRB submissions.
Maintain investigator site files and manage ongoing regulatory affairs.
Ensure compliance with GCP, study protocols, and investigational product handling.
Communicate with sponsors and regulatory authorities, including during audits and inspections.
Participant Recruitment & Study Conduct:
Recruit and enroll eligible subjects into clinical trials.
Coordinate and schedule study-related procedures and appointments.
Administer questionnaires, cognitive tests, vital signs, and EKGs as required.
Data & Specimen Management:
Collect accurate, verifiable data for case report forms and study databases.
Assist with collection, handling, and shipping of laboratory specimens per protocol.
Study Close-Out & Documentation:
Coordinate study close-out activities and ensure proper documentation.
Support manuscript writing and editing for journal or conference submission (optional but preferred).
Offsite & Administrative Duties:
Attend investigator meetings and sponsor-related events (limited travel).
Perform offsite tasks such as dry ice pickup for specimen transport.
Experience Level
Intermediate Level
Pay and Benefits
The pay range for this position is $43.26 - $45.67/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 Mableton,GA.
Application Deadline
This position is anticipated to close on Aug 1, 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.
Salary : $43 - $46