Job Title: Clinical Trials Disclosure Manager - Unlock the Power of Transparency in Healthcare
Job Description:
Join Amgen, a pioneering biotechnology company, as a Clinical Trials Disclosure Manager and play a vital role in driving transparency and innovation in healthcare. As a key member of our team, you will lead the preparation of clinical regulatory documents for public disclosure, ensuring compliance with international regulations and company requirements.
Your mission will be to:
Prepare and anonymize clinical regulatory documents for public disclosure, protecting personal and commercially confidential information
Collaborate with cross-functional stakeholders to define redaction strategies, implement redactions, and ensure submission readiness
Manage projects, prioritize work, and meet internal and external deadlines
Support trend analysis and continuous improvement initiatives to drive transparency and efficiency
To succeed in this role, you will need:
A Master's degree and 4-6 years of pharmaceutical industry experience, or equivalent
Minimum 2 years of experience in preparing regulatory documents for public disclosure
Familiarity with international regulations, guidances, and best practices on clinical transparency and disclosure
Excellent communication, leadership, and project management skills
At Amgen, we offer a competitive salary, a dynamic work environment, and opportunities for growth and development. As an Equal Opportunity employer, we are committed to diversity, inclusion, and providing reasonable accommodations for individuals with disabilities.
Ready to join us? Click Apply Now to start your journey with Amgen today!
Apply Now
Join Amgen, a pioneering biotechnology company, as a Clinical Trials Disclosure Manager and play a vital role in driving transparency and innovation in healthcare. As a key member of our team, you will lead the preparation of clinical regulatory documents for public disclosure, ensuring compliance with international regulations and company requirements.
Your mission will be to:
Prepare and anonymize clinical regulatory documents for public disclosure, protecting personal and commercially confidential information
Collaborate with cross-functional stakeholders to define redaction strategies, implement redactions, and ensure submission readiness
Manage projects, prioritize work, and meet internal and external deadlines
Support trend analysis and continuous improvement initiatives to drive transparency and efficiency
To succeed in this role, you will need:
A Master's degree and 4-6 years of pharmaceutical industry experience, or equivalent
Minimum 2 years of experience in preparing regulatory documents for public disclosure
Familiarity with international regulations, guidances, and best practices on clinical transparency and disclosure
Excellent communication, leadership, and project management skills
At Amgen, we offer a competitive salary, a dynamic work environment, and opportunities for growth and development. As an Equal Opportunity employer, we are committed to diversity, inclusion, and providing reasonable accommodations for individuals with disabilities.
Ready to join us? Click Apply Now to start your journey with Amgen today!
Apply Now