Careers
Join Our Team
We are looking for passionate people to join our growing team. View our career opportunities below and apply today.
Open Positions
Headlands Research is looking for a licensed Nurse Practitioner to join our team as we run cutting edge clinical research trials.
The ideal candidate is:
- Passionate about clinical trials and making a difference
- A team player who can collaborate and move at a fast pace
Duties:
- Provides patient consultations and education in an outpatient setting under the direction of the physician in charge of the clinical trial
- Conducts study-related physical exams and follow-up visits
- Reviews and adheres to assigned research study protocol
- Works with the study-leading physician in evaluation and review of potential study participants’ eligibility
- Maintains proper documentation
- Ensures that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
- Collaborates with multidisciplinary team members
- Reviews lab results imaging reports, and other study-specific reports
Requirements / Qualifications:
- Graduate of an accredited school of nursing school
- Current Practice Registered Nurse (PRN)
- Current provider card in Basic Life Support (BLS)
- Minimum of 1 to 2 years of experience in a similar role
- Strong computer skills, including Microsoft Word, Excel, and PowerPoint
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.
Duties:
- 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/Qualification/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
PLUS
- 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
Headlands Research is looking for a Clinical Research Assistant to assist coordinators in clinical research protocols. This individual will work directly with the coordinators, investigators, and other research staff to ensure protocol visits are being completed in accordance with protocol guidelines.
Qualifications:
- Clinical Research Experience is preferred though not required.
- Interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources.
- Knowledge in medical terminology and laboratory skills a plus
- Accuracy, attention to detail and ability to set priorities and meet deadlines
- Knowledge with Microsoft office a plus
Duties:
- To assist research coordinators in conducting clinical trials. Responsibilities include but are not limited to:
- Collect clinical data: vital signs, telephone calls and entering data into electronic data system
- Screening and enrolling study subjects based on inclusion/exclusion criteria
- Verifying study documents
Headlands Research Brownsville
Contact Us
Whether you want to learn more about our clinical trials or you have a general clinical study question, we want to hear from you. Please complete the form below.