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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 RoleESSENTIAL 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
MINIMUM QUALIFICATIONS AND EDUCATION REQUIREMENTS
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.
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
Duties
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:
Experience and training in conducting clinical trials with knowledge of ICH GCP
OR
Two years of college in a health-related program or LPN
OR
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