Subinvestigator- Physician Assistant or Nurse Practitioner

Celerion; Tempe (AZ); On-site; USD 90,000 - 120,000; Part time

Job summary

Celerion in Tempe, AZ is seeking a licensed clinician (Nurse Practitioner, Physician Assistant, or MD/DO) to conduct clinical studies per protocol, review safety data, and monitor participant safety under the Principal Investigator.

Responsibilities include screening exams, reviewing medical histories and tests, managing adverse events, counseling participants, and coordinating with nursing staff and study management to ensure successful protocol execution.

Qualifications

• 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.
• Spanish language skills a plus.

Responsibilities

• Maintain timely compliance with SOPs, study documents, and trainings.
• Assist with training of new staff.
• Create a friendly environment for study participants.
• Produce accurate study data while ensuring participant safety.
• Review safety data and monitor adverse events.
• Conduct screening physical examinations and eligibility decisions.
• Counsel participants regarding abnormal tests.
• Attend Sponsor SIVs and coordinate with nursing/study management.
• Provide training to clinic associates as needed.
• Review outside medical records and SUSAR reports when requested.
• Flexible schedule with 10+ hours per week (Fri-Mon possible).

Skills

Communication

Organizational skills

Attention to detail

Customer service

Team player

Flexible hours

Spanish language skills

Education

Nurse Practitioner/PA/MD/DO

Job description

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.

Essential Functions

• 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
• A flexible schedule that could include Friday - Monday (start times may vary between 7am and 8am) for a minimum 10 hours a week

Knowledge/Skills/Education/Licenses

• 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
• Spanish language skills a plus

Celerion Values: Integrity Trust Teamwork Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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