Clinical Senior Project Leader - Mid/Large BioPharma (Select EU countries)

Parexel; Uxbridge; Remote; GBP 90,000 - 130,000; Full time

Benefits offered by this job

Holiday

Pension plan

Car allowance (country specific)

Job summary

Parexel in the United Kingdom is seeking an experienced Senior Project Leader (Senior Clinical Project Manager) to lead delivery for mid to large bio/pharma clients globally.

You will provide cross-functional leadership across trials, manage study plans, budgets, risk, and client relationships, ensuring quality and adherence to ICH GCP. This role offers remote home-based working across the UK and other EMEA locations with a competitive salary and benefits.

Qualifications

• Bachelor’s degree or equivalent; science/medical field preferred.
• Strong CRO experience and Phase I–III project management.
• Excellent command of English.
• Financial management and client relationship skills; bid defense experience is a plus.

Responsibilities

• Develop and maintain a formal project plan with milestones, budgets and resources.
• Perform initial and ongoing risk management.
• Ensure first-time quality of deliverables.
• Own and manage the client relationship at study level.
• Understand and manage the project P&L including invoicing and change in scope.
• Lead cross-functional project team and represent in client meetings.
• Contribute to SOP reviews and other organizational initiatives.

Skills

Project leadership

Risk management

Client communication

Quality-focused

Team leadership

Problem solving

Attention to detail

Cross-functional collaboration

MS Office

Education

Bachelor’s degree in Science or Medical field

Tools

MS Excel

PowerPoint

MS Word

MS Project

Job description

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 Senior Project Leader to lead project delivery to our Mid & Large BioPharma clients and their projects on a global level. You will ideally have Therapeutic Area expertise in a combination of the following: Oncology plus any of the following Ophthalmology, Neurology, Dermatology or NASH.

This position is available in the following EMEA locations - UK, Ireland, Poland, Romania, Spain, Italy, Hungary, Croatia, Lithuania and we offer fully remote (country stipulated) home 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.

Key Accountabilities

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.

Perform Initial And Ongoing Risk Management

• Identify potential project risks and implement contingency plans, mitigate actual risks with team members and keep client informed about risks and contingencies.

Manage and ensure first time quality on the project deliverables:

• Establish quality standards for the project that drive individual and team commitment to quality.

Develop And Manage The Client Relationship

• Owns the client relationship at a study level and responsible for client communication ensuring high client satisfaction.

Understand And Own The Project P&L

• Manage the project according to budget with revenue recognition and forecasting, including resource management, pass-through management (review, regular reconciliation and forecasting) as well as managing Change in Scope and all all project invoicing activities.

Manage The Cross-functional Project Team

• 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.

Other Assigned Responsibilities

• 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.

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 Phase I, II-III clinical trial project management with demonstrable project leadership skills are essential.
• In-depth knowledge of the Therapeutic Areas due to our current resource needs: Oncology is essential plus any of the following Ophthalmology, Neurology, Dermatology, NASH are desirable.
• Strong command of written and spoken English language is essential.
• Strong financial management and client relationship skills as well as involvement with bid defense activities 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, (car allowance is country specific) and a benefits package including holiday, pension and other leading-edge benefits that you would expect with a company of this type.