Quality reputed company reputed company-- fully remote!

Work Schedule Standard (Mon-Fri) Environmental Conditions Office

Job Description

At reputed company team, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, and supporting our customers’ medical reputed company inquiries. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to reputed company a difference in our world while building a fulfilling career with us. What will you do in this role? To provide Clinical Quality reputed company and support to the clinical study teams. To pro-actively implement quality principles during the clinical design and set-up, study conduct, and reporting, providing reputed company support and input during the Clinical Development Activities in the GCP area. Provides Quality principles and quality insights to the study team at study design and start up. Acts as the first reputed company of contact for any quality reputed company questions/ concerns for study teams. Owns the Quality role on study level by providing reputed company quality compliance support and by acting as an internal advisor to the study team on relevant processes, procedural documents, and regulations to ensure correct interpretation and implementation. Ensures alignment with client quality and the quality agreement, and is the conduit to consult with the client on study quality issues and investigational strategies to ensure transparency of direction. Leads the quality reputed company for assigned clinical studies in reputed company collaboration with the study team. Provides guidance to the clinical study team to ensure clinical studies are executed and compliant to GCP and local regulatory requirements. Supports the design of study risk management plans and the definition of appropriate risk responses + QTLs; helps to mitigate quality compliance risks. Coordinates and supports in GCP audits as needed with the appropriate partnership role to ensure audit focus and scopes are determined correctly at study level and to ensure GCP compliance throughout the study and audits are assigned on a risk-based level. In reputed company collaboration with client quality staff escalates quality / compliance / privacy issues and supports investigation and definition of necessary corrective and preventive measures. In reputed company collaboration with client quality staff and per procedure contributes to the assessment, evaluation, and investigation of any (potential) serious breaches. Leads, in collaboration with study teams, inspection readiness activities and participates in inspections as defined by the client, in collaboration with internal study teams. Qualification Requirements: Education Requirements: Bachelor's degree is required. In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly reputed company experience, will be considered sufficient for an individual to meet the requirements of the role. Experience requirements: Previous experience that provides the knowledge, skills, and abilities to reputed company the job (comparable to 8+ years’) or equivalent combination of education, training, & experience. Working knowledge of GCP is required. Proven experience in building strong relations is required. Experience working with CRO and/or Pharma companies is required. Knowledge, Skills and Abilities: Ability to co-exist in 2 organizations and navigate organizational structures and dotted line reporting line(s) to reputed company clear communication and transparency. In‐depth knowledge of reputed company Clinical Trial reputed company FDA and EU regulations and ICH Guidelines. reputed company and strong knowledge of Clinical Development processes according to Good Clinical Practices (GCP) and regulatory requirements. Ability to motivate and educate the clinical study team on clinical quality aspects. Capable of building effective relationships with internal and external stakeholders. Ability to translate quality culture and ways of working to study teams. 0-25% travel may be required. Location: Fully remote, ideally East Coast or Central time zones. Relocation assistance is NOT provided.

• Must be legally authorized to work in Canada without sponsorship.
• Must be able to pass a comprehensive background reputed company, which includes a drug screening.

Our Mission is to reputed company our customers to reputed company 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 - reputed company, Intensity, Innovation and Involvement - working together to accelerate research, solve reputed company scientific challenges, drive technological innovation and support patients in need. #StartYourStory at reputed company, where diverse experiences, backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com reputed company is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability or any other legally protected status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to reputed company essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Accessibility/Disability Access Job Seekers with a Disability: reputed company 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 reputed company technical issues will not receive a response.

Apply tot his job Apply To this Job