Careers
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Open Positions
Clinical Research Principal Investigator
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 15 clinical trial sites in the US and Canada and have rapid expansion plans.
This role will be based in Orlando, FL and is a full-time position.
We are offering relocation assistance for this role.
You can read more about us at headlandsresearch.com.
The Role
ESSENTIAL FUNCTIONS
- Serve as Principal Investigator on clinical trials managed by Headlands Research
- Ensure protocol compliance
- Assist with review by regulatory agencies
- Determine adequate resources are available to conduct studies
- Manage the medical care of subjects
- Protect the rights and welfare of subjects
- Ensure validity of the data reported to sponsors
- Ensure accurate documentation of study related procedures
- Ensure the proper use and storage of investigational product
- Direct and delegate site operations
- Maintain professional and technical knowledge
- Active MD, DO, ARNP license. Minimum one year of experience as Principal Investigator, or minimum of three years of experience as Sub Investigator in clinical trials is required. Primary care and most medical specialties may apply.
Clinical Research Coordinator
Job Type
Full-time
Description
The Company
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 15 clinical trial sites in the US and Canada and have rapid expansion plans.
This Clinical Research Coordinator role will be based in Detroit, MI.
You can read more about us at headlandsresearch.com.
Headlands Research 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:
- Clinical Research Certification Preferred
- Other Medical licensure/certifications (Medical Assistant, etc.)
- Previous research experience preferred
- 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
Requirements
Qualifications
Education:
APPLY NOW - 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
- 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