Nurse Practitioner

Location: San Antonio, TX, USA

Notice

This position is no longer open.

Requisition Number: 2555

Position Title: Nurse Practitioner

External Description:

SUMMARY: Worldwide Clinical Trials is a top-notch CRO focused on early-stage clinical trial development. We are hiring a people-focused, high-energy, Nurse Practioner to join our growing team of clinical researchers in San Antonio, TX.

About Worldwide Clinical Trials, Early Phase: Located in San Antonio, TX, Worldwide’s Clinical Pharmacology Unit (CPU) focused on providing superior customer service to our sponsor. Worldwide Clinical Trials has been top-ranked by its early phase customers for these qualities in the latest Early Phase CRO Quality Benchmarking Report by Industry Standard Research, making it the go-to CRO for your early phase program. Founded by physicians we are focused on offering an uncommon experience to our employees and our customers.

About You: You are a forward-thinking, people-focused Nurse Practioner with a passion for making a difference in the research industry. You have experience reviewing subjects/patients' medical charts, conducting physicals, and reviewing a subject/patient's medical history. Additionally, you will have your FNP license, and have at least 3 years of experience as a Nurse Practioner.

 Responsibilities:

Tasks may include but are not limited to:

  • Responsible for reviewing and clarifying volunteers’ medical histories/medications and for conducting physical exams to help determine their eligibility for study enrollment according to protocol specifications.
  • Conducts physical examinations and assists in determining volunteers’ eligibility for study enrollment according to protocol specifications.
  • Obtains, and prepares certain laboratory specimens as defined in the study protocol and as assigned by WCT Management.
  • Assesses Laboratory results, ECG tracings to determine subject eligibility with Physician Investigator oversight
  • Monitors and assesses the health status and response to treatment of subjects during their course of study participation.
  • Evaluates adverse events reported by study subjects and/or research staff and then communicates findings to the Principal Investigator.
  • Provides medical expertise and support to research staff members for the successful implementation of clinical trials.
  • Reviews screening tools and other study-related documents as requested by research staff.
  • Shares in the day-to-day training and direction of research staff pertaining to basic research processes, new therapeutic areas, and study-specific requirements.
  • Performs other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive

 Requirements:

  • Required: Bachelor's and Master’s Degree and completion of an American Medical Association-approved Nurse Practitioner program.
  • Current “Nurse Practitioner Permit” (license) through the Texas Board of Nursing. Minimum of five (5) years experience in clinical practice as a Nurse Practitioner Or Bachelors's and Master’s Degree and completion of an American Medical Association-approved Physician’s Assistant program. Current PA license through the Texas Board of Nursing. Minimum of five (5) years experience in clinical practice as a Physician’s Assistant.

Preferred:    

  • Two (2) years of clinical research experience. Proficiency in women’s health care/exams.

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City:

State: Texas

Employment Type: Regular

Community / Marketing Title: Nurse Practitioner

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: San Antonio, Texas US

CountryEEOText_Description: Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. Worldwide is committed to working with and providing reasonable accommodations to applicants with disabilities. We are proud to be an equal opportunity workplace where people thrive by being themselves and are inspired to do their best work every day.

 Worldwide Clinical Trials does not accept unsolicited resumes from 3rd party vendors

© Worldwide Clinical Trials 2023

We only accept resumes from staffing organizations with pre-approved contractual agreements. Please do not forward resumes directly to our hiring managers, jobs alias, or any other company location. Unsolicited resumes from employment agencies will not be considered and Worldwide is not responsible for any fees related to unsolicited resumes.