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Clinical Research Associate- Copenhagen, Denmark
Pharmaceutical Product Development (PPD)
Copenhagen, Denmark
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.
A day in the Life:- 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 Danish and English
- 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
- 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 Danish and English
- 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
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Accessibility/Disability Access
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
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Job posted: 2023-03-06
