Advanced Practice Provider - Sub Investigator

Pinnacle Clinical Research; Texas; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical, dental, vision, long term/dis

3 weeks of paid time off

Tranquility Room (locations apply)

Pinnacle Gym (locations apply)

Scrub voucher

Job summary

Pinnacle Clinical Research is seeking an Advanced Practice Provider to join as a sub-investigator in Houston, TX. The role focuses on follow-up visits, lab review, subject recruitment, and collaboration with the clinical operations team.

The candidate will operate under study protocols, ensure patient safety, and coordinate with physicians, nurses, and sponsor representatives. A graduate degree and an APRN/PA license are required; GCP training is preferred.

Qualifications

• Advanced degree from graduate school; and one to two years related experience and/or training.
• Current APRN or PA license is required.
• GCP training certification preferred.
• Valid driver’s license required.

Responsibilities

• Works with affiliates or collaborating research sites.
• Maintains confidentiality and complies with sponsor requirements and regulatory guidelines.
• Performs study procedures including physical exams, consent, subject history, adverse events, and vital signs.
• Reviews study activities and protocols to ensure compliance with regulations and SOPs.
• Assists in preparation for study monitor visits and site inspections.
• Performs subject screening and recruitment.
• Coordinates multiple projects with competing priorities and deadlines.

Skills

Written and oral communication

Organizational skills

Attention to detail

Interpersonal skills

Education

Advanced degree (APRN/PA)

GCP training certification (preferred)

Tools

Microsoft Office

Internet Explorer

Google Chrome

Mozilla Foxfire

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Advanced Practice Provider - Sub Investigator

Houston, TX, US

3 days ago Requisition ID: 1092

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:

• 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

knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software.

Work Environment and Physical demands:

• 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:

• Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
• 3 weeks of paid time off
• 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