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Full-time
postgraduate degree, professional certificate
401k, Medical insurance, Dental insurance, Vision insurance, Long term disability, Short term disability
Posted 14d ago
~40 hrs/week
Responsibilities
The Advanced Practice Provider will serve as a sub-investigator, responsible for conducting study-related procedures, reviewing labs, and managing patient follow-up visits. They will also assist in subject recruitment, ensure protocol adherence, and coordinate with the clinical operations team.
Requirements
Candidates must hold an advanced degree from a graduate school and possess a current advanced registered nurse practitioner or physician assistant license. One to two years of related experience and bilingual proficiency in English and Spanish are required.
Full job description
Summary: The Clinical Research Nurse Practitioner/Physician Associate will be listed as a sub-investigator on all ongoing study protocols. She/He will be a key member of the team and will be responsible for seeing follow up visits, reviewing labs for study subjects, recruiting subjects into protocols, and working with the clinical operations team.
Duties and Responsibilities:
Works with affiliates or collaborating research sites.
Maintains subject and document confidentiality at all times and understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration, good clinical practice, International Conference on Harmonization, Health Insurance Portability and Accountability Act, Institutional Review Boards, and institutional policies and procedures.
Performs study related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments.
Reviews and holds expert knowledge of study related activities and protocols.
Adheres to study protocols, Food and Drug Administration regulations, and good clinical practices at all times.
Assists in the preparation for study monitor visits.
Performs subject screening and recruitment.
Exercises judgement within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the principal investigator.
Interacts with internal and external personnel such as physicians, nurses, administration staff, industry sponsor representatives, central laboratory and imaging personnel, and clinical trial patients.
Coordinates multiple projects with competing priorities and deadlines as needed based on clinical trial protocol directives and study volume.
Education/Experience:
Advance degree from a graduate school; and one to two years related experience and/or training; or equivalent combination of education and experience. Specialized training.
Certificates and Licenses:
Current advanced registered nurse practitioner or physician assistant license.
Valid driver’s License
GCP Training certification preferred
Knowledge, Skills, and Other Abilities:
Bilingual (English/Spanish) required
Written and oral communication skills
Organizational skills
Ability to pay attention to detail
People skills including possessing a positive, friendly, and professional demeanor
Ability to be flexible with changing priorities
Ability to communicate in a diplomatic and professional manner
Strong interpersonal skills
Strong mathematical knowledge
Excellent computer skills
knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.
Work Environment and Physical demands: The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Work is performed in an office/laboratory and/or a clinical environment.
• Exposure to biological fluids and/or bloodborne pathogens.
• Personal protective equipment is required such as protective eyewear, garments, and gloves.
• Occasional travel may be required domestic and/or international.
• Ability to work in an upright and/or stationary position for 6-10 hours per day.
• Frequent mobility required.
• Occasional squatting, kneeling, or bending.
• Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.
Perks of working at Pinnacle Clinical Research:
• 401k
• Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
• 3 weeks of paid time off
• 13 paid company holidays
• Tranquility Room (specific locations apply)
• Pinnacle Gym (specific locations apply)
• Scrub voucher (specific positions apply)
And more! Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved
At Pinnacle Clinical Research, we are driven by a shared mission to improve lives through innovation in clinical trials. As a premier clinical research network, we specialize in conducting high-quality, patient-focused studies across a broad range of therapeutic areas, with particular expertise in liver disease, metabolic disorders, memory loss, and neurodegenerative conditions.
With a growing national footprint, Pinnacle partners with leading sponsors, CROs, and healthcare providers to accelerate medical breakthroughs and bring tomorrow’s treatments to today’s patients. Our experienced investigators, diverse patient populations, and commitment to operational excellence enable us to consistently deliver rapid enrollment, reliable data, and exceptional retention.
We believe clinical research should be both rigorous and compassionate. That’s why we prioritize patient education, cultural sensitivity, and community engagement at every site. From first-time volunteers to experienced participants, every individual is treated with dignity, transparency, and care.
Whether you’re a sponsor looking for a high-performing site network, a physician exploring clinical trial collaboration, a patient seeking new treatment options or someone interested in a rewarding career in clinical research, we invite you to connect with us and be part of advancing the future of medicine.
Offices: 5109 Medical Dr, San Antonio, Texas 78229, US · 8015 Shoal Creek Blvd, 114, Austin, Texas 78757, US · 3201 S Austin Ave, 335, Georgetown, Texas 78626, US · 2502 W Trenton Rd, Edinburg, Texas 78539, US · 717 N Expressway 77/83, 6-9, Brownsville, Texas 78520, US
How many Science & Research jobs are open in Houston, TX right now?
There are currently 1,617 open science & research positions in Houston, TX listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Houston, TX?
Companies currently hiring include McWilliams School of Biomedical Informatics at UTHealth Houston, Oscorp Industries Consulting, Texas Children's Hospital, St. Luke's Health, Amentum, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Houston, TX?
Yes — 213 of the 1617 open science & research positions offer remote or hybrid work (83 remote, 130 hybrid).
How do I apply for Science & Research jobs in Houston, TX?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.