Subinvestigator

Subinvestigator

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 Celerions 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

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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