Start-up Specialist and Contract Specialist
- Employer
- Labcorp
- Location
- Lisbon, Portugal
- Salary
- Competitive
- Start date
- 14 Aug 2022
- Closing date
- 12 Sep 2022
View more
- Discipline
- Clinical Research, Clinical Operations
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
If you are looking to take on responsibility and leverage your know-how in the start-up phase of clinical trials - ensuring a successful start of important clinical studies in the UK -, this is the perfect opportunity. You will be working alongside our dedicated and supportive team of SSU experts and exclusively for one of our renowned international sponsors - in a role that allows you to have a real impact on people's health and lives.
What we have to offer: a strong international support network, flexible working solutions that facilitate a genuine work-life balance, a highly competitive compensation package and the opportunity to significantly raise your profile in the industry.
Your tasks:
- Serve as the primary contact for investigative sites, proactively managing site activation and providing guidance for your sites during the start-up phase of your assigned studies
- Ensure that all assigned maintenance and start-up activities are on track and in accordance with client expectations, ICH / GCP, SOPs, budget, quality and all applicable local laws and guidelines
- Collect, track and perform a quality review of all essential and investigator documents required for effective and compliant study site activation and maintenance
- Liaise with our regulatory department regarding document submission requirements and ensure documents required are collected and submitted on time. Ensure high quality documents are filed and systems are updated on an ongoing and timely basis, taking ownership for compliance and audit readiness
- Escalate any issues with submissions and / or approvals for your assigned studies appropriately and in a timely fashion, both to internal departments and to external stakeholders such as Institutional Review Boards (IRBs), Independent Ethics Committees (IECs) and UK regulatory authorities
- Customize country and site specific patient Informed Consent Forms to ensure compliance with local requirements and protocol
- Support the negotiation of site contracts and budgets with study sites and track progress of contract and budget milestones / developments, intervening and escalating as appropriate
Education:
- Degree in a relevant field such as pharmacology, life sciences, clinical trial management, (veterinarian) medicine, health care (management), nursing, chemistry, biology, oecotrophology etc.,
- In lieu of the above, an equivalent completed vocational education or equivalent professional experience
Experience:
- Solid expertise in clinical trials within a CRO or a pharmaceutical company with a specialization in clinical study start up / regulatory processes
- Demonstrated understanding of research protocol requirements as well as the ability to communicate them / educate others about them
- Proven track record collaborating successfully with operational project teams as well as external investigative sites and local regulatory authorities (including IRBs and IECs)
- In-depth experience with submissions to the UK regulatory authorities - observing all local regulations and guidelines as well as international standards such as ICH and GCP
- Familiarity with investigator start-up documents and contract / budget negotiation processes with study sites
- Autonomous work style with excellent time and project management skills
- Business fluency in English - both spoken and written - is a must
REMOTE
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement .
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.
For more information about how we collect and store your personal data, please see our Privacy Statement .
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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