Altasciences
Physician Assistant Clinical Researcher
Altasciences, Cypress, California, United States, 90630
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 Sub-Investigator is responsible for supervising clinical activities for the clinical trial to which they are assigned. The Sub-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). 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 in compliance 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. What You'll Need To Succeed
PA degree from an accredited Physician Assistant Program; or NP degree from an accredited Nurse Practitioner Program; or MD/DO from an accredited Medical School Medical Degree for an accredited Physician program Must be ACLS certified Current Basic Life Support (BLS, CPR/AED) certification Minimum of 5 years of previous experience working in the clinical research industry as an Investigator/Sub-Investigator Comprehensive understanding and application of all aspects of clinical research in the opinion of the Director of Medical Operations, Medical Director and/or General Manager What We Offer
The pay range estimated for this position is $125,000 to $180,000 per year. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data. 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 Altasciences' Incentive Programs Include: Training & Development Programs Employee Referral Bonus MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
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 Sub-Investigator is responsible for supervising clinical activities for the clinical trial to which they are assigned. The Sub-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). 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 in compliance 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. What You'll Need To Succeed
PA degree from an accredited Physician Assistant Program; or NP degree from an accredited Nurse Practitioner Program; or MD/DO from an accredited Medical School Medical Degree for an accredited Physician program Must be ACLS certified Current Basic Life Support (BLS, CPR/AED) certification Minimum of 5 years of previous experience working in the clinical research industry as an Investigator/Sub-Investigator Comprehensive understanding and application of all aspects of clinical research in the opinion of the Director of Medical Operations, Medical Director and/or General Manager What We Offer
The pay range estimated for this position is $125,000 to $180,000 per year. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data. 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 Altasciences' Incentive Programs Include: Training & Development Programs Employee Referral Bonus MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!