Full Job Description
This role is ideal for a PA/NP who is interested in the clinical research industry and is currently working other casual or part-time positions and has the flexibility to work primarily weekday morning (0700) and occasional weekend morning shifts
Casual Physician Assistant (PA) or Nurse Practitioner (NP) Are you looking for a new fresh way to use your medical skills in a team that is focused on true patient interaction and NOT on pressured schedules that are unrealistic and burdensome? If that sounds great to you, read on. The Medical Department at Nucleus Network – USA continues to grow and is looking for casual mid-level providers to join this dedicated team of PAs, NPs and MDs. Nucleus Network has secured its global positioning as the only dedicated Phase 1 clinical trials provider with facilities across the United States, Australia, London, and the United Kingdom. Make an impact by helping to ADVANCE MEDICINE and IMPROVE LIVES in this rewarding and fun position.
Key Responsibilities
- Providing high quality medical services to participants of clinical trials conducted by Nucleus Network in accordance with FDA Code of Federal Regulations, clinical trial protocols, ICH/GCP and Standard Operating Procedures (SOPs) and all relevant ethical and legal requirements (including the Declaration of Helsinki) with respect to clinical trials.
- To provide and document informed consent to potentially eligible participants and ensure that NO screening procedures occur before a valid Informed Consent Form (ICF) has been signed.
- Ensuring participants are consented to the correct ICF including part of study.
- Conduct and document medical histories and physical examinations at screening appointments to ensure only potentially eligible participants are enrolled in studies at NN.
- Reviewing and signing relevant documentation (i.e. clinical lab reports, diagnostic results, inclusion /exclusion criteria) in order to deem participants eligible to enrol in studies at NN.
- If required, contacting PCP / Specialists for further medical information of participants to assess their eligibility.
- To medically manage healthy volunteers involved in clinical trials conducted at NN.
- Performing required medical activities as indicated in the Protocol, i.e. Physical examinations, Neuro exams, C-SSRS evaluations, Injection site reactions, Adverse Event evaluation, etc.
- Conduct outpatient visits for participants who are currently in a trial.
- Participating in the review of individual adverse events for accuracy and clinical importance, and characterize their relationship to the study drug while assessing severity and seriousness
- Understanding the potential adverse reactions of all clinical trials being conducted.
- When required, participate in administration of investigational products and on-study activities
- Work collaboratively with all functional departments including Project Management, Recruitment, Resourcing, Screening, Pharmacy, and QA Departments.
Requirements
- Medical Practitioner (licensed or eligible PA or NP ), with qualifications from a recognized institution.
Preferred Qualifications
- Ability to work well within a multi-disciplinary team (which includes clinical and non-clinical staff) is critical
- Enthusiastic, and possess excellent communication and clinical skills to facilitate and build good rapport with clinical trial participants
- Previous experience with conducting early phase clinical trials is viewed upon favourably but not essential
- Recent (within 1 year) clinical experience – new graduates with strong medical background encouraged to apply
- Flexible schedule with the understanding that evenings (rare), weekends, and a rotating holiday schedule are expected with advanced notice.
Job Types: Part-time, Temporary
Pay: $65.00 per hour
Work Location: In person
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