When our values align, there's no limit to what we can achieve. Parexel is in the business of improving the world’s health.
We do this by providing a suite of biopharmaceutical services that help clients across the world transform scientific discoveries into new treatments.
We believe in our values, We are currently looking to recruit an experienced to lead project delivery and oversight to our and their projects on a global level.
This position is available in the following EMEA locations -and we offer fully remote (country stipulated), hybrid or office-based working.
As the will actively lead the Parexel and client teams by combining your deep clinical research experience with insight into client pressures in order to develop the right solution for the client.
You will provide overall cross-functional leadership of our clinical trials and studies as well as the project teams to achieve operational excellence and deliver projects on time, to budget, with the highest quality as well as being compliant with ICH GCP to meet client expectations.
Key Accountabilities:- Develop and maintain a formal project plan with all key milestones, budgets, and resources assigned to specific tasks and outcomes.
Identify potential project risks and implement contingency plans, mitigate actual risks with team members and keep client informed about risks and contingencies.
Establish quality standards for the project that drive individual and team commitment to quality.- Owns the client relationship at a study level and responsible for client communication ensuring high client satisfaction.
Manage the project according to budget with revenue recognition and forecasting, including resource management, pass-through management (review, regular reconciliation and forecasting).
Enable all stakeholders to achieve successful study completion while maintaining high client satisfaction.- Represent Project Leadership Function in external client meetings and presentations such as Bid Pursuit Meetings, Investigator Meetings or others as required.
May include non-billable work such as SOP review and lead or contribute to other organizational initiatives.
Education:- Bachelor’s degree or equivalent level of education (Science or Medical related field preferred) or proven substantial clinical project management experience.- Advanced degree desirable.
Skills:- Ability to take a proactive, solutions-based approach.- Critical thinking & problem-solving.- Excellent interpersonal, verbal and written communication skills.- Highly accountable with a strong client focus.- A flexible attitude with respect to assignments and new learning.- Ability to manage multiple and varied tasks with enthusiasm and be able to prioritize workload with high attention to detail.- Ability to work in a matrix environment and to value the importance of teamwork and collaboration.- Basic understanding of all aspects of the project life cycle.- Ability to work independently with oversight guidance.- Proficient in Microsoft Excel, Power Point, and Word, and project planning software.
Knowledge and Experience:- Strong previous CRO experience and understanding of either with demonstrable skills are essential.- In-depth knowledge in any therapeutic areas (TA's) are welcome.
There is a strong preference for a combination of the following areas due to our current resource needs: , or therapeutic expertise.- Strong command of written and spoken English language is essential.
An additional language is a benefit.- Previous with involvement in - Strong and skills are essential.- Applications from candidates with pharma experience may also be considered. - Familiarity with standard business and e Clinical systems used in Clinical Research is desirable.- ICH and GCP regulations in relevant geographies.- Solid clinical knowledge and understanding of clinical research and protocol design.
In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry.
Your hard work will be rewarded with a competitive salary, bonus and a benefits package including holiday, pension and other leading-edge benefits that you would expect with a company of this type.
reklama
Senior Project Leader - Enterprise (select Eu Countries), Czech Republic
Czech Republic, Czech Republic, Czech Republic
Publikováno 2024-10-01
Vyprší 2024-10-04
ID #2372343437
Free
Senior Project Leader - Enterprise (select Eu Countries), Czech Republic
Czech Republic, Czech Republic, Czech Republic,
Publikováno October 1, 2024
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PAREXEL International is a leading global biopharmaceutical services provider, which continues to be a premier, trusted partner to clients who rely on the Company for expertise and flexibility, as well as the efficiencies of a worldwide infrastructure, to help them more quickly achieve their development and commercialization goals. For 30 years, PAREXEL has complemented client organizations with strategic insight, deep scientific knowledge, tactical expertise, and a wealth of experience throughout the development process. The Company's offerings include worldwide regulatory expertise, Phase I-IV clinical research services, eClinical technologies that accelerate development, and integrated commercialization services. PAREXEL is focused on providing tailored solutions that match a client's specific needs by applying the right blend of resources and capabilities, as well as the right guidance and high level of quality needed to help them bring safe and effective treatments to patients sooner.
Headquartered near Boston, Massachusetts, PAREXEL operates in over 70 locations throughout more than 50 countries, and has over 11,000 employees worldwide.
Visit www.PAREXEL.com for more information.
Specialties
Regulatory and product development consulting,
early phase clinical research,
phase II-III clinical research,
late phase clinical research,
eClinical solutions,
patient and site recruitment,
clinical logistics,
flexible outsourcing models,
strategic partnering