UpTrials is a new platform to help nurses find clinical research roles. We are partnered with an organization seeking a Clinical Research Nurse Practitioner to join our team onsite in San Antonio, TX! To be considered for this and other roles, please create a profile at app.uptrials.com.
The Clinical Research Coordinator (CRC) / Nurse Practitioner manages the daily operations of clinical trials while serving as a Sub Investigator on clinical trials and performing medical assessments. Other responsibilities include but are not limited to: train and manage study-related staff, oversee preparation for study conduct and ensure necessary approvals and documentation are in place, communicate with sponsors, investigators, and participants, perform study-related procedures such as informed consent and data collection, perform phlebotomy and lab duties, manage study supplies, laboratory procedures, and closeout activities.
Our partner is a a growth-oriented research company focused on excellent conduct of clinical trials. We are team-oriented and core value-centric. We value Focus, Discipline, and Accountability. We offer benefits and a competitive salary. We do excellent work and are Making Life Better.
Open to Relocation
Yes
Job Seniority
Senior
Job Roles and Responsibilities
Phlebotomy
Patient Visits
Spanish Speaking (Bilingual)
Good Clinical Practice (GCP)
Nurse Practitioner
CRC
Sub Investigator
Therapeutic Areas
Primary Care
Vaccines
Work Authorization
Required
Requirements
Essential Qualifications:
2+ years Clinical Research experience
Nurse Practitioner Licensure - TX
Bilingual
Experience with phlebotomy and laboratory procedures
Ability to make sound medical judgements in relation to clinical research protocols
Proficiency in performing medical procedures and assessments
Self motivated, team player with strong attention to detail & ability to multitask
Strong verbal and written communication skills
Ability to travel up to 15% between San Antonio site locations
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