Principal Investigator

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.

The Principal Investigator is responsible for the supervision and delegation of the tasks related to the clinical trial they are Principal Investigator of. The Principal Investigator 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).

You'll Do Here

• Supervise the clinical activities for the clinical trial they are Principal Investigator.
• Delegation of trial related tasks and the review of employees on the Delegation of Authority and Signature Log per job title/training record.
• Perform protocol training.
• Provide documentation for the Sub-Investigators.
• 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.
• 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.
• Record and follow-up on adverse events and determine causality.
• Report serious adverse events to appropriate parties.
• 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.
• Participate in sponsor visits and regulatory audits.
• May act as Sub-Investigator on studies not assigned to them as Principal Investigator.

• MD degree from an accredited Physician Program and Advanced Cardiac Life Support (ACLS) certification required.
• Previous experience with similar responsibilities; ideally related to the industry.

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

• Health/Dental/Vision Insurance Plans
• 401(k)/RRSP with Employer Match
• Paid Vacation and Holidays
• Paid Sick and Bereavement Leave
• Employee Assistance & Telehealth Programs

Altasciences’ Incentive Programs Include:

• Training & Development Programs
• Employee Referral Bonus Program

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