Clinical Site Liaison FSP Poland
Clinical Site Liaison FSP Poland
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Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific youll 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.
Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out across commercial and government contracts. Together we help clients define and develop clinical programs minimize delays and execute high-quality cost-efficient clinical studies.
The PPD FSP Solution:
PPDs Functional Service Provider division partner with and serve as an extension of our PPD team supporting our customers key functions. We cover customer needs on every level allowing them to do more with less with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.
Joining within our PPD FSP functional area allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.
The Clinical Site Liaison (CSL) is a field based expert who supports the conduct and the patient recruitment of global clinical trials at investigative sites through local and relational support.
The successful candidate will have clinical trial operational experience and deep understanding of patient pathways and trial recruitment. Proven expertise in engaging building and maintaining excellent working relationships with country / region specific investigative sites KOLs site networks and Patient Advocacy groups (PAG). From within the Trial Operations (Trial Ops) team closely work together with the clinical trial/ indication teams and with CROs and other vendors. Collaborate with the Global Patient Advocacy (GPA) group as well as with the Medical Affairs group(MSLs).
ROLES AND RESPONSIBILITIES:
- Participate in neurology franchise and study-level feasibility activities through providing key country/ regional and site specific knowledge including patient pathways and operational execution.
- Interface and act as a local TrialOps representative an expert on the clinical trial protocol(s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trials.
- Lead and engage in local site KOL and network engagement initiatives in view of the clinical trials.
- Contribute to the trial specific site feasibility / selection strategy and collaborate with the Clinical Trial Team (CTT) and CRO to support the site start-up process as needed.
- Facilitate with the site contractnegotiation/signatureas needed collaborate with the GloSaM group
- Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site eg the Principal Investigator (PI) and site preferences and best practices on clinical trials standard of care treatments competing studies etc. Ensure a supportive relationship with clinical sites and trial personnel.
- Proactively work to fully understand the patient voice preferences and pathway(s). Closely work with the GPA team. Speak to patient groups and support groups live events and conferences as allowed by local / regional guidance. May also attend live and virtual patient events to assist in responding to questions about the client the trial(s) and other information on Mode of Action (MOA).
- May participate in monitoring oversight activities such as accompanying the CRO CRA during site visits. This to ensure high quality conduct and execution of the clinical trials according to the protocol and ICH GCP and local regulatory requirements.
- Closely work together with the Medical Affairs colleagues eg the MSLs to ensure optimal synergies in the respective site contacts and support.
- Optimize site engagement for a specific trial and across the neurology franchise to ensure site engagement and quality for the site-level enrollment and execution of every trial.
- Oversee and track patient recruitment for the regional sites and pro-actively identify ways to prevent recruitment delays
- Pro-actively identify issues and look for solutions in the assigned clinical trial and timely escalate them to the respective study CTM CODL Global Head of Clinical Site Communication Recruitment and Liaisons Head of Trial Operations and/or Senior Management as needed
- Identify efficiencies best practices and lessons learnt and ensure they are shared acrosstrials/indications/compounds
- Search for and embrace innovation
- May be asked to provide input to the clinical development strategy/plan
- Participate in workstreams and provide input to procedures/SOPs/WIs and related documents
SKILLS AND COMPETENCIES
- Knowledge of ICH-GCP and other applicable legislation
- Ability to quickly understand complex neurological disease areas treatments and clinical development plans
- Understand the healthcare therapeutic landscape patient pathways and investigative sites
- Excellent communication and presentation skills and relationship management of multiple stakeholders internally and externally including sites KOLs networks PAGs CROs and others
- Leadership with the ability to overcome challenges seek opportunities to remove barriers influence without authority
- Highly developed organizational skills problem solving analytic and able to prioritize
- Experience with tools and systems for managing clinical studies
EDUCATION EXPERIENCE AND QUALIFICATIONS
- Bachelors degree Scientific or health related field University degree medical or para-medical (MD Biology Biomedical Sciences Pharmacy Veterinary etc.) or equivalent by experience
- Minimum of 6 years of experience in Biotech / pharma preferably in roles including site engagement and / or clinical trial monitoring experience
- Valid drivers license.
- Ability for travel nationally and occasional international travel.
- Experience in global clinical trials is a plus
- Prior experience in Neurology Auto-immune and rare disease background
Employment Type
Full-Time
