All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. We are searching on behalf of our customer Pfizer in Finland a talent for a Site Relationship Partner role.
You will be the main Pfizer point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety at the investigator site.
You will be responsible for site monitoring and oversight and building and retaining relationships from site activation through the lifecycle of studies. As part of the oversight responsibilities, you will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks.
You will also be accountable for identifying CRA performance issues and ensure appropriate corrective and preventative actions are put in place.
You will be “the face of Pfizer" and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and Pfizer’s reputation is that of “Partner of Choice."
You will proactively collaborate and provide local intelligence to country outreach surveys, targeted sites strategies, study design, and Pfizer pipeline opportunities. You will be accountable for study start up, activation, and execution to the plan for targeted sites. In addition, for being the main point of contact, the lead will help coordinate with other roles and functions that will interface with target sites, thereby, simplifying site Pfizer communications and enhancing overall visibility into and confidence of quality of site-level activities.
You will report to Director of Clinical Operations and coordinate with institutions and investigators at the local level.
A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology
Solid knowledge of clinical development processes with strong emphasis on monitoring
Demonstrated ability to oversee a 3rd party and/or demonstrated ability in Quality Assurance
Site Management/Monitoring (CRA) experience
Project management experience preferred in the clinical development area
Ability to lead, troubleshoot and influence for delivery
Demonstrated knowledge of quality and regulatory requirements for applicable countries
Demonstrated knowledge of site intelligence at country/cluster level in support of site recommendation
Demonstrated knowledge of clinical trial methodology and the drug development process, related to monitoring clinical trials, GCP, FDA, or country-specific regulatory environment
Demonstrated experience in site activation
Ability to communicate effectively and appropriately with internal & external stakeholders
Ability to evaluate, interpret and present complex issues and data to support assessment and mitigation of site risk
Challenges people to surpass themselves in reaching their objectives using innovative solutions
Fluent communication skills in English and in Finnish (other Nordic languages is a plus)
A chance to partner with colleagues of diverse backgrounds and abilities, people who contribute to all aspects of what Pfizer does
You will be a part of a business with 90 000 global colleagues working towards a healthier world. In Finland, you have about 120 engaged colleagues
Pfizer values diversity and working together to make breakthroughs that change patients´ lives
Pfizer is an employer that encourages wellness and work-life balance
A chance to be a part of a company that cares for its colleagues through an inclusive workplace that fosters a sense of community, encourages innovation
Location: Finland, remote work possible, travelling necessary
Extent: Full time
Agreement: Fixed term agreement for 12 months at a time with possibility of renewal initially via StaffPoint
Start date: ASAP
Please apply by registering your CV and cover letter in English along with your salary request as soon as possible.
Our selection process is continuous, and the advert may close before the recruitment process is completed if we have moved forward to the screening or interview phase.
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