Clinical Research Medical Director, Obesity/ Cardiovascular
US - California - Thousand Oaks - Field/Remote
Career Category
Clinical DevelopmentJob Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like youâre part of something bigger, itâs because you are. At Amgen, our shared missionâto serve patientsâdrives all that we do. It is key to our becoming one of the worldâs leading biotechnology companies. We are global collaborators who achieve togetherâresearching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. Itâs time for a career you can be proud of.
Clinical Research Medical Director
Live
What you will do
Letâs do this. Letâs change the world. In this vital role you will serve as clinical expert to provide clinical/scientific knowledge into the development, delivery and communication of the global scientific/medical evidence plan for the assigned indication(s).
- Provide clinical/scientific knowledge into the development, design, delivery and communication of the global evidence generation plan for Cardiovascular and Obesity programs.
- Support cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program
- Participate and provide clinical input into safety and regulatory interactions
- Interpret and communicate clinical trial data
- Author clinical study reports, 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 Global Development Lead
- Provide clinical content input to materials to be used in Scientific Affairs as well as the Commercial Organization
- Contribute to TPP (target product profile) and Global Product Safety (GPS) development
- Create development options and present to Global Dev Review Committee (GDRC), Therapeutic Area Governance (TAG)
- Interact with TA leadership and extended team to develop options
- Interact with Center for Design Analysis (CfDA), Center for Observational Research (CfOR), Clinical Pharmacology Modeling & Simulation (CPMS), etc., to bring innovative later development options
Win
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 teaching and patient care activities
- Strong and versatile clinical development experience in endocrinology or cardiology and accreditation in relevant sub-specialty
- Knowledge of pharmaceutical âŚ
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Field/Remote
Benefits/PerksAnnual bonus program Career development Career development opportunities Comprehensive employee benefits Comprehensive employee benefits package Discretionary annual bonus Financial plans Flexible Spending Accounts Flexible work models Health and welfare plans Life and Disability insurance Professional and personal growth Remote work Retirement and Savings Plan Stock-based long-term incentives Time-off plans Total Rewards Plan Welfare plans
Tasks- Communication
- Develop key opinion leaders
- Provide clinical expertise
Biopharmaceutical Biostatistics BioTech Biotechnology Cardiology Cardiovascular Clinical Development Clinical Pharmacology Clinical Research Clinical Study Reports Clinical Trial Design Clinical trials Communication Data interpretation Diabetes Endocrinology Evidence Generation FDA FDA regulations GCP Good clinical practices Insurance Interpersonal Leadership Matrix Environment Medical Writing Obesity Observational Research Organization Pharmaceutical Presentation Problem-solving Product Development Publications Regulatory Interactions Regulatory Submissions Research Sales Scientific communication Scientific Knowledge Simulation
Experience3 - 5 years
Education TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9