Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Office

Job Description

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

• Proactively collaborates with initiative leads and senior management to develop, optimize and improve processes, associated systems/applications, training and communications.
• Provides guidance and support to teams in successfully identifying, analyzing, and addressing potential operational study risks.
• Strategically develops and leads large scale, complex process improvement initiatives.
• Proactively identifies and collates information required to assess compliance with processes and to prioritize business process improvement needs.
• May review, assess and update procedural documents for overall compliance with current processes.
• Performs special projects, assignments and administrative tasks per business needs.
• Mentors, coaches, and supports team members in developing and implementing process improvement initiatives.

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).
• Significant clinical research experience in all phases of clinical study life cycle, including start-up, interim and close-out, is preferred.

• Strong judgment, decision making, issue resolution and risk management skills.
• Broad understanding of procedural documents
• Mature investigative and analytical skills
• Familiarity with the practices, processes, and requirements of clinical trials
• Broad understanding of clinical management technology and systems, and strong digital literacy
• Strong ability to influence
• Effective oral and written communication skills including the ability to communicate in English, both orally and in writing
• Capable of advising and promoting collaboration in a multi-disciplinary and/or multi-cultural team setting
• Broad understanding of regulatory guidelines and directives