At Headlands Research, we are building the best clinical trial company in the world. We’re an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation. Founded in 2018, our company is in high growth mode; we operate 11 clinical trial sites in the US and Canada and have rapid expansion plans.
This new Clinical Research Coordinator role will be based in Stockbridge, GA
This opening is for (Monday-Friday) and (Full time).
You can read more about us at headlandsresearch.com.
(CRA Headlands) is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines.
The ideal candidate:
Has worked as lead coordinator and managed trials from start up to close out.
Has experience in submitting regulatory & creating source documents
Worked in multi-therapeutic clinical trials; has a license/certificate to administer vaccine
Comprehend study design of each protocol that is assigned
Perform procedures in compliance with the study protocol
Recruit and screen study subjects according to specific protocol requirements
Collect and record study data in source documents via electronic system (CRIO)
Manage study related activities
Adherence to protocol requirements
Review laboratory data
Assess and document compliance
Manage investigational product
Assess, record, and report Adverse Events as outlined in the protocol
Manage/train ancillary staff
Experience and training in conducting clinical trials with knowledge of ICH GCP
Two years of college in a health-related program or LPN
Bachelor’s degree in a health or scientific related program
A thorough understanding of regulatory requirements (this would include ICH GCP guidelines.. (if they are a research assistant they know what that is. This is what all clinical trials are governed by.)
Excellent interpersonal and communication skills
Able to interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
Experience with CRIO (Clinical Trial Management System) is a plus
Experience with administering vaccines is a plus
Internal Number: 002
About Headlands Research
At Headlands Research, we are creating the best clinical trial research company in the world. We are an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation.
You can read more about us at headlandsresearch.com and see some of our recent work featured on the national news at http://headlandsresearch.com/news.html.
Founded in 2018, our company is in high growth mode; we already operate eleven clinical trial sites in the US and Canada, with more to come.
As we rapidly expand, we are looking for talented and dynamic clinical trial research professionals to join our team - and we'd love to hear from you!