Career Category
Clinical Development
Job Description
Join Amgens Mission of Serving Patients
At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.
Since 1980 weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology Inflammation General Medicine and Rare Disease we reach millions of patients each year. As a member of the Amgen team youll help make a lasting impact on the lives of patients as we research manufacture and deliver innovative medicines to help people live longer fuller happier lives.
Our award-winning culture is collaborative innovative and science based. If you have a passion for challenges and the opportunities that lay within them youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Clinical Research Medical Director Cardiometabolic
What you will do
Lets do this. Lets change the this vital role you will support the development execution and communication of the global scientific / medical evidence plan. Support cross-functional and global collaborations to integrate broad medical scientific and commercial input into the development program. Support the development of key scientific external relationships with opinion leaders. Participate and providing clinical input into safety and regulatory interactions.
Provide clinical / scientific input during the development and execution of clinical trials
Interpret clinical trial data
Participate in safety assessments
Participate in interactions with regulatory agencies
Author CSRs publications and regulatory submissions
Develop key opinion leaders and make scientific presentation at advisory boards key scientific meetings and external committee meetings as delegated by GDL
Identify new clinical research opportunities
Support in-licensing and out-licensing activities and partner relationships
Support product lifecycle management for new indications as directed by Global Development Leader
Provide clinical content input to : regulatory interactions and documents safety interactions and documents materials to be used in Scientific Affairs and materials to be used by the Commercial Organization
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.
Basic Qualifications :
MD or DO degree from an accredited medical school
AND
2 years of clinical research experience and / or basic science research
Preferred Qualifications :
Three (3) or more years of clinical research experience in the biopharmaceutical industry (biotech pharmaceutical or CRO company)
Five or more years of clinical research experience and / or basic science research combined with clinical instructing and patient care activities
Strong and versatile clinical development experience in endocrinology or cardiology and accreditation in relevant sub-specialty
Knowledge of pharmaceutical product development product lifecycle and commercialization processes
Experience with developing study concepts for clinical development and clinical trial designs with cross functional input including biostatistics observational research and patient reported outcomes in Phase 1 2 and / or 3 clinical trials in obesity or diabetes
Knowledge of Good Clinical Practices (GCP) FDA and EMEA / CHMP regulations and guidelines and applicable international regulatory requirements
Leadership experience / potential as a medical expert in a complex matrix environment
Ability to effectively present ideas and document complex medical / clinical concepts in both written and oral communication
Strong interpersonal skills and problem-solving abilities while exhibiting superior judgment and a balanced realistic understanding of issues and resolution path
What you can expect of us
As we work to develop treatments that take care of others we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture well support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to relevant skills experience and qualifications.
In addition to the base salary Amgen offers a Total Rewards Plan based on eligibility comprising of health and welfare plans for staff and eligible dependents financial plans with opportunities to save towards retirement or other goals work / life balance and career development opportunities that may include :
Apply now and make a lasting impact with the Amgen team.
In any materials you submit you may redact or remove age-identifying information such as age date of birth or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Sponsorship
Sponsorship for this role is not guaranteed.
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 and live the Amgen values to continue advancing science to serve patients. Together we compete in the fight against serious disease.
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 disability status or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Salary Range
261969.00 USD - 329723.00 USD
Required Experience :
Director
Key Skills
EMR Systems,Post Residency Experience,Occupational Health Experience,Clinical Research,Managed Care,Primary Care Experience,Medical Management,Utilization Management,Clinical Development,Clinical Trials,Leadership Experience,Medicare
Employment Type : Full-Time
Experience : years
Vacancy : 1
Monthly Salary Salary : 329723 - 329723
Medical Director • Thousand Oaks, California, USA