Subinvestigator- Physician Assistant or Nurse Practitioner

Celerion•Tempe, AZ

14d•Onsite

About The Position

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Job Purpose: Conduct clinical studies according to study protocols, review safety data and monitor the safety of study participants enrolled into clinical trial protocols under the supervision of the Principal Investigator.

Requirements

Excellent oral and written communication skills
Proven organizational skills, ability to multi-task and manage multiple priorities
Demonstrates attention to detail
Strong customer service and interpersonal skills
Team player with the ability to work collaboratively
Willingness and ability to work flexible hours including weekends and holidays to ensure clinic coverage
Nurse Practitioner, Physician Assistant, or MD/DO
Eligible to obtain DEA certificate upon hire.
Training in Basic Life Support and Advance Cardiac Life Support, or willing to obtain upon hire
Board certified or board eligible in a primary care specialty, i.e. family practice, internal medicine, E.R. medicine or as a PA-C or NP, or MD/DO
1 year medical experience and / or clinical research experience

Nice To Haves

Spanish language skills a plus

Responsibilities

Maintain timely compliance with Celerion’s SOPs, required study documents, and other study- specific mandatory trainings
Assist with training of new staff upon achieving personal proficiency in required skills and tasks.
Create a friendly and welcoming environment to study participants
Produce accurate and timely study data while ensuring participant safety
Participate in the ICF process by answering any volunteer questions about the study, in collaboration with the investigator as needed.
Conduct screening physical examinations
Review subject screening data, including subject medical histories, ECGs, laboratory studies, and any other ancillary tests as outlined by the study protocol.
Make preliminary eligibility decisions based on protocol inclusion and exclusion criteria.
Counsel participants regarding abnormal tests and make referrals in collaboration with the investigator as necessary
Attend Sponsor SIVs
Assist in the logistical setup of new studies by collaborating with the nursing department and working with study management to ensure the successful execution of all medical aspects of the protocol
Provide training to clinic associates as needed
Resolve queries
During study Review safety-related data including ECGs, AEs, laboratory data or other ancillary tests in a timely manner
Conduct physical examinations
Perform minor procedures as outlined by the protocol following completion of required training
Engage with client in-person (on-site) or via written, electronic or telephone correspondence to address any medical-related issues
Ensure safety of study participants by reviewing and managing adverse events and serious adverse events under the supervision of the PI.
Perform assessments and administer necessary treatment when required
Assist in referring participants to specialists as necessary
Review of outside medical records if requested by the investigator
Review of SUSAR reports if requested by the investigator
Review safety-related data including ECGs, AEs, laboratory data or other ancillary tests in a timely manner
Conduct physical examinations
Resolve queries