17 days old

Patient Safety Agreement Management - Manager

Amgen
Thousand Oaks, CA 91360
  • Job Code
    116889966
Amgen

Job ID: R-90011
Location: Thousand Oaks, CA, US 91360

Amgen is seeking a Patient Safety Agreement Manager to join our team and work from Amgen's beautiful Thousand Oaks, CA campus. To learn more about this position:

The Patient Safety Agreement Management team act as a hub for the safety and regulatory aspects of business partnerships and strategic alliances, from inception through implementation and maintenance. The team ensures that safety agreements for our business partnerships and other commercial alliances are robustly documented and managed, implemented efficiently and effectively, in line with operational objectives and capabilities.

The Patient Safety Agreement Manager reports to Director, Patient Safety Agreement Management and will provide operational support for day to day PSAM activities.

Key Activities

- Supports business partner safety agreement monitoring

- Assists in triaging and handling requests from business partners and internal stakeholders

- Provides project management support for operational meetings (OMTs) with business partners

- Supports business partner pharmacovigilance audits as required

- Supports development of process related documentation to ensure compliance

- Performs other duties related to the position as necessary as defined in Standard Operating Procedures or as requested by his/her supervisor

- Undertakes activities delegated by the EU QPPV as detailed in the PV System Master File and maintains a state of inspection readiness

Knowledge and Skills

- Good attention to detail
- Good organization and time management skills
- Good written and oral communication skills
- Capable of creative problem solving
- Ability to envision and implement business process solutions

- Strong collaboration skills with good customer focus

- Demonstrates flexibility, adaptability and sense of accountability

- Demonstrated ability to build relationships and work cross-functionally
- Ability to successfully prioritize a diverse workload to meet deadlines

- Knowledge of Regulatory and Safety functional activities

Basic Qualifications:

Doctorate degree

OR

Master's degree and 2 years of directly related experience

OR

Bachelor's degree and 4 years of directly related experience

OR

Associate's degree and 10 years of directly related experience

OR

High school diploma / GED and 12 years of directly related experience

Preferred Qualifications:

Masters degree and 4 years or more experience

Experience working as a paralegal

Experience working in pharmacovigilance or in a project management role

Amgen provides a collaborative and creative culture in a company with a strong track record of innovation. Our culture encourages open dialogue and diverse views to land on the best solutions, and we help ensure our staff are equipped to excel today and tomorrow.

Amgen focuses on areas of high unmet medical needs and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

PI116889966

<b>Amgen</b><br/><br/><b>Job ID: </b>R-90011<br/><b>Location: </b>Thousand Oaks, CA, US 91360<br/><br/>Amgen is seeking <b>a Patient Safety Agreement Manager</b> to join our team and work from Amgen's beautiful Thousand Oaks, CA campus. To learn more about this position: <br><br>The Patient Safety Agreement Management team act as a hub for the safety and regulatory aspects of business partnerships and strategic alliances, from inception through implementation and maintenance. The team ensures that safety agreements for our business partnerships and other commercial alliances are robustly documented and managed, implemented efficiently and effectively, in line with operational objectives and capabilities. <br><br>The Patient Safety Agreement Manager reports to Director, Patient Safety Agreement Management and will provide operational support for day to day PSAM activities.<br><br>Key Activities<br><br>- Supports business partner safety agreement monitoring<br><br>- Assists in triaging and handling requests from business partners and internal stakeholders<br><br>- Provides project management support for operational meetings (OMTs) with business partners<br><br>- Supports business partner pharmacovigilance audits as required<br><br>- Supports development of process related documentation to ensure compliance<br><br>- Performs other duties related to the position as necessary as defined in Standard Operating Procedures or as requested by his/her supervisor<br><br>- Undertakes activities delegated by the EU QPPV as detailed in the PV System Master File and maintains a state of inspection readiness<br><br>Knowledge and Skills<br><br>- Good attention to detail<br>- Good organization and time management skills<br>- Good written and oral communication skills<br>- Capable of creative problem solving<br>- Ability to envision and implement business process solutions<br><br>- Strong collaboration skills with good customer focus<br><br>- Demonstrates flexibility, adaptability and sense of accountability<br><br>- Demonstrated ability to build relationships and work cross-functionally<br>- Ability to successfully prioritize a diverse workload to meet deadlines<br><br>- Knowledge of Regulatory and Safety functional activities<br><br><b>Basic Qualifications:</b><br><br>Doctorate degree<br><br>OR<br><br>Master's degree and 2 years of directly related experience<br><br>OR<br><br>Bachelor's degree and 4 years of directly related experience<br><br>OR<br><br>Associate's degree and 10 years of directly related experience<br><br>OR<br><br>High school diploma / GED and 12 years of directly related experience<br><br><b>Preferred Qualifications: </b><br><br>Masters degree and 4 years or more experience<br><br>Experience working as a paralegal <br><br>Experience working in pharmacovigilance or in a project management role<br><br><b> Amgen </b> provides a collaborative and creative culture in a company with a strong track record of innovation. Our culture encourages open dialogue and diverse views to land on the best solutions, and we help ensure our staff are equipped to excel today and tomorrow. <br><br><b> Amgen </b> focuses on areas of high unmet medical needs and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. <br><br>Join Us <br> <br> If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. <br> <br> Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. <br> <br> As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. <br> <br> Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.<br/><br/> <img src="https://analytics.click2apply.net/v/Ma1wd2sDnGgycoMyuQ5Jl"> <p>PI116889966</p>

Categories

Posted: 2020-01-07 Expires: 2020-02-07

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Patient Safety Agreement Management - Manager

Amgen
Thousand Oaks, CA 91360

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast