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Clinical Research Coordinator
Actalent • Atlanta, GA 30309 • Posted 2 days ago
Clinical Research Coordinator
Actalent • Atlanta, GA 30309 • Posted 2 days ago
In-person • Full-time • $58,000-$64,000/yr • Mid Level
Description:
Seeking a detail‑oriented and motivated Clinical Research Coordinator (CRC) to support ongoing clinical trials in neurology. The CRC will work closely with investigators, clinical staff, and research sponsors to ensure studies are conducted in accordance with protocols, regulatory requirements, and institutional standards.
Key Responsibilities:
+ Coordinate day‑to‑day operations of clinical research studies, including participant recruitment, screening, enrollment, and follow‑up.
+ Serve as a primary point of contact for study participants, investigators, sponsors, and regulatory bodies.
+ Conduct informed consent discussions and ensure proper documentation.
+ Schedule study visits, assessments, imaging, and laboratory procedures.
+ Collect, record, and maintain accurate study data in electronic data capture systems.
+ Ensure compliance with study protocols, Good Clinical Practice (GCP), and FDA regulations.
+ Prepare and submit regulatory documents, IRB submissions, amendments, and continuing reviews.
+ Manage study supplies, investigational products, and equipment as required.
+ Assist with monitoring visits, audits, and sponsor communications.
+ Maintain organized study files and documentation for internal and external review.
+ Support the development and implementation of new research protocols.
Qualifications:
+ Bachelor's degree in a health‑related field (e.g., biology, neuroscience, psychology, public health) preferred.
+ Prior experience in clinical research or healthcare strongly preferred.
+ Knowledge of GCP, FDA regulations, and clinical trial operations.
+ Strong organizational skills with the ability to manage multiple tasks and deadlines.
+ Excellent communication and interpersonal skills for working with patients and multidisciplinary teams.
+ Proficiency with electronic medical records and research data systems.
+ Certification as a Clinical Research Coordinator (CCRC) is a plus but not required.
Job Type & Location
This is a Permanent position based out of Atlanta, GA.
Pay and Benefits
The pay range for this position is $58000.00 - $64000.00/yr.
Health Insurance - Medical, Vision, Dental PTO
Workplace Type
This is a fully onsite position in Atlanta,GA.
Application Deadline
This position is anticipated to close on Feb 13, 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 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Seeking a detail‑oriented and motivated Clinical Research Coordinator (CRC) to support ongoing clinical trials in neurology. The CRC will work closely with investigators, clinical staff, and research sponsors to ensure studies are conducted in accordance with protocols, regulatory requirements, and institutional standards.
Key Responsibilities:
+ Coordinate day‑to‑day operations of clinical research studies, including participant recruitment, screening, enrollment, and follow‑up.
+ Serve as a primary point of contact for study participants, investigators, sponsors, and regulatory bodies.
+ Conduct informed consent discussions and ensure proper documentation.
+ Schedule study visits, assessments, imaging, and laboratory procedures.
+ Collect, record, and maintain accurate study data in electronic data capture systems.
+ Ensure compliance with study protocols, Good Clinical Practice (GCP), and FDA regulations.
+ Prepare and submit regulatory documents, IRB submissions, amendments, and continuing reviews.
+ Manage study supplies, investigational products, and equipment as required.
+ Assist with monitoring visits, audits, and sponsor communications.
+ Maintain organized study files and documentation for internal and external review.
+ Support the development and implementation of new research protocols.
Qualifications:
+ Bachelor's degree in a health‑related field (e.g., biology, neuroscience, psychology, public health) preferred.
+ Prior experience in clinical research or healthcare strongly preferred.
+ Knowledge of GCP, FDA regulations, and clinical trial operations.
+ Strong organizational skills with the ability to manage multiple tasks and deadlines.
+ Excellent communication and interpersonal skills for working with patients and multidisciplinary teams.
+ Proficiency with electronic medical records and research data systems.
+ Certification as a Clinical Research Coordinator (CCRC) is a plus but not required.
Job Type & Location
This is a Permanent position based out of Atlanta, GA.
Pay and Benefits
The pay range for this position is $58000.00 - $64000.00/yr.
Health Insurance - Medical, Vision, Dental PTO
Workplace Type
This is a fully onsite position in Atlanta,GA.
Application Deadline
This position is anticipated to close on Feb 13, 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 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.