Senior Project Leader - Biotech (Select EU countries)

at  Parexel

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, Patients First, Quality, Respect, Empowerment & Accountability.
We are currently looking to recruit an experienced Project Leader or Senior Project Leader’ to lead project delivery and oversight to our Biotechclients and their projects on a global level. You will ideally have Therapeutic Area expertise in a combination of the following: Oncology, Ophthalmology, Neurology or Dermatology.
This position is available in the following EMEA locations - UK, Ireland, Poland, Romania, Italy, Spain, France, Serbia, Hungary, Czech Republic, Netherlands, Lithuania and we offer fully remote (country stipulated), hybrid or office-based working.
As the Senior Project Leader (Senior Clinical Project Manager) you 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.

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 Early Phase and/or Phase II-III clinical project management with demonstrable project leadership 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: Oncology, Ophthalmology, Neurology or Dermatology therapeutic expertise.
• Strong command of written and spoken English language is essential. An additional language is a benefit.
• Previous CRO experience is strongly preferred with involvement in bid defense activities.
• Strong financial management and client relationship skills are essential.
• Applications from candidates with pharma experience may also be considered.
• Familiarity with standard business and eClinical 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.

INDEPENDENTLY RESPONSIBLE FOR ALL PROJECT LEADER TASKS AND DELIVERABLES ACCORDING TO SOPS ON ASSIGNED PROJECTS:

• Develop and maintain a formal project plan with all key milestones, budgets, and resources assigned to specific tasks and outcomes.

OTHER ASSIGNED RESPONSIBILITIES:

• May include non-billable work such as SOP review and lead or contribute to other organizational initiatives.