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Clinical Trials Disclosure Associate

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Clinical Trials Disclosure Associate

India - Hyderabad Apply Now
JOB ID: R-205348 LOCATION: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Feb. 24, 2025 CATEGORY: Clinical

Clinical Transparency & Disclosure Associate

Role Name: Clinical Transparency & Disclosure Sr. Associate

Department Name: Global Regulatory Affairs & Strategy (GRAAS)

Role GCF: 3

Hiring Manager Name: Jennifer Vande Weghe

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

Roles & Responsibilities:

  • Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with regulatory requirements and the agreed strategy defined by the cross functional team
  • Ensure consistent quality across documents, ensure submission readiness, and hand off for timely submission or posting
  • Collaborate with team members to resolve problems and escalate issues
  • Record and maintain written redaction strategy for the study and product
  • Manage timelines and coordinate work across team

Required Skills:

  • Experience understanding and interpreting data/information and its practical application
  • Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through
  • Ability to follow controlled processes
  • Excellent spoken and written English
  • Project management skills, including ability to prioritize work in order to meet required deadlines
  • Problem solving ability

Basic Qualifications:

  • Bachelor’s degree
  • Minimum of 1 year experience working with regulatory documents in a biotech/ pharmaceutical environment
  • Familiarity with clinical research and clinical regulatory documents
  • Knowledge of clinical trial disclosure regulations, guidelines, and best practices

Preferred Qualifications:

  • One year experience preparing regulatory documents for public disclosure

EQUAL OPPORTUNITY STATEMENT

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

We will ensure that individuals with disabilities are provided with 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 an accommodation.

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