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
As a Sub-Investigator I, you will be at the forefront of clinical research, supervising and driving the success of clinical trials. Your key responsibilities include promoting and upholding Good Clinical Practices (GCP) and ensuring the smooth execution of clinical investigations. You will be the guardian of patient rights, data integrity, and protocol compliance, ensuring that our clinical trials meet and exceed regulatory standards and industry best practices.
What You'll Do Here
- Your primary responsibility is to ensure the safety and well-being of our research participants. This involves reviewing laboratory results, conducting vital sign assessments, and monitoring safety tests, among other critical tasks.
- Supervise the clinical activities for the clinical trial they are assigned.
- You'll be responsible for recording and meticulously following up on adverse events, demonstrating your commitment to subject welfare.
- Your role will involve making crucial trial-related decisions, helping to guide the course of our clinical trials to successful outcomes.
- Uphold strict adherence to study protocols, verifying that our research results are reliable and meaningful.
- 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.
- Verify that all requirements for obtaining informed consent are met, respecting the rights and autonomy of our research subjects.
- Perform physical examinations, take detailed medical histories, and conduct reviews that contribute to the comprehensive understanding of each patient's health status.
- Be available on-site for protocol-required surveillance and remain on-call to address medical events as they arise.
- Play an active role in sponsor visits and regulatory audits, showcasing your dedication to compliance and quality research.
- Record all study-related events with impeccable compliance to GCP, ensuring the accuracy and transparency of our records.
- Review study protocols and standard operating procedures (SOPs) to stay aligned with the latest research practices.
- Complete and review regulatory documents as required, showcasing your commitment to compliance.
What You'll Need to Succeed
- Hold an PA degree from an accredited Physician Assistant Program and maintain an Advanced Cardiac Life Support (ACLS) certification.
- Experience related to the responsibilities of this role, demonstrating your commitment to the industry and your ability to excel in it.
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes
- Health/Dental/Vision Insurance Plans
- 401(k)/RRSP with Employer Match
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Employee Assistance & Telehealth Programs
- Telework when applicable
- Training & Development Programs
- Employee Referral Bonus
- Job Family P-8
- Pay Type Salary
- Cypress, CA, USA