YOUR NEW COMPANY!

At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences.
We are better together and together We Are Altasciences.

ABOUT THE ROLE

The Specialized Nurse Practitioner is responsible for supervising clinical activities for the clinical trial to which they are assigned. The Nurse Practitioner will promote Good Clinical Practices (GCP) during the conduct of clinical investigations by ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of data generated at the site and directing the conduct of the clinical investigation according to regulation/guidance and standard operating procedure (SOP).

WHAT YOU’LL DO HERE

• Supervise the clinical activities for the clinical trial they are assigned.
• Ensure subject safety at all times, this may include but is not limited to: review of clinical laboratory results and/or other test results.
• Review and/or performance of vital signs, ECGs or other safety tests.
• Record and follow-up on Adverse Events.
• Perform critical trial related tasks and/or make trial related decisions during the course of the trial.
• Ensure subject eligibility is met based on protocol inclusionary/exclusionary criteria and that the subject continues to meet eligibility criteria throughout the course of a clinical trial.
• Ensure requirements related to obtaining informed consent are met.
• Perform physical examinations and medical history intake and review.
• Be on-site for surveillance as required by protocol and remain available on-call for medical events.
• Participate in sponsor visits and regulatory audits.
• Document study related events incompliance with GCP.
• Review study protocols and SOPs.
• Complete and/or review regulatory documents as applicable.
• May act as Principal Investigator on studies at the discretion of the Chief Medical Officer, Medical Director or Senior Principal Investigator and study sponsor.