CRA (Level II) - Client dedicated
Posted 1 day 3 hours ago by Thermo Fisher Scientific
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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.
Location/Division Specific Information:
Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Our Danish office consists of colleagues with in-depth therapeutic experience, people with various educations within life science and both newly educated people plus people with years of experience. All in all, we have a very dynamic environment where initiative, flexibility, responsibility, commitment, and fun are in focus.
Discover Impactful Work:
PPD clinical research service s mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams.
Perform and coordinate all aspects of the clinical monitoring and site management process
Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation
Manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.)
Act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability
Ensure audit readiness
Develop collaborative relationships with investigational sites
Keys to Success:
Education
- Bachelor's degree in a life science related field or a registered nursing certification or equivalent and relevant formal academic/vocational qualification Knowledge,
Skills, Abilities
- Valid driver's license
- Well-developed critical thinking skills, including but not limited to: in-depth investigator for appropriate root cause analysis and problem solving
- Good oral and written communication skills - both English and Danish/Swedish
- Good listening skills, attention to detail and the ability to perceive customers' underlying issues
- Good organizational and time management skills
- Effective social skills
- Ability to remain adaptable in a wide range of scenarios
- Ability to work in a team or independent as required
- Good digital literacy - Microsoft office plus the ability to learn appropriate software