AbbVie is a leading pharmaceutical company dedicated to discovering and delivering innovative medicines that address serious health issues today and anticipate the medical challenges of tomorrow. Our work culture is centered around making a remarkable impact on people's lives, focusing on key therapeutic areas such as immunology, oncology, neuroscience, eye care, and Allergan Aesthetics portfolio. We are committed to excellence in research and development to improve patient outcomes worldwide.

As a Senior Clinical Research Associate at AbbVie, you will play a vital role in ensuring successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of studies. Your responsibilities will include overseeing site-related study execution activities like monitoring visits, site evaluations, selection, activation, close out reports, and ensuring adherence to federal regulations and Good Clinical Practices (GCPs). You will maintain clinical trial management systems with up-to-date site-specific information while providing local regulatory expertise.

In this role, you will also be responsible for coaching and mentoring CRAs for their development and may act as the country point of contact for CROs. You may participate in global/local task forces or initiatives and identify training needs while standardizing training solutions for SMM monitors globally. With guidance, you may serve as a key point of contact at the country/district level for assigned studies. Additionally, you will be responsible for remote data review of assigned sites/studies according to the Integrated Data Review Plan (IDRP) within study timelines.

The ideal candidate should have a Bachelor's or equivalent degree in a health-related field (e.g., Medical, Scientific), with at least 3 years of site monitoring experience. Strong analytical skills are required to evaluate complex issues effectively. Excellent interpersonal skills with flexibility in communication are essential along with demonstrated business ethics and integrity. If you are looking to join an organization dedicated to transforming healthcare through cutting-edge research and innovation while fostering professional growth opportunities, we invite you to apply for this position as a Senior Clinical Research Associate at AbbVie.

Key Job Requirements:

• Bachelors or equivalent degree in a health-related field preferred
• Minimum 3 years of site monitoring experience

Skills:

• - Strong planning and organizational skills
• - Flexibility and adaptability to changing requirements
• - Proactive team player mindset

Seniority Level: Specialist-Level

• Senior

Job Functions: Cybersecurity

• Clinical Research

Industries : Information Technology

• Pharmaceuticals