Clinical Project Leader – Senior Project Leader, Mid/Large BioPharma

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Oversee project execution for Mid & Large BioPharma clients and their global initiatives.

• Lead teams from Parexel and clients, leveraging clinical research expertise and awareness of client challenges.

• Provide comprehensive cross-functional leadership for clinical trials, studies, and project teams.

• Ensure projects are completed on schedule, within budget, with exceptional quality, and in adherence to ICH GCP standards.

• Create and maintain detailed project plans that encompass milestones, budgets, resources, tasks, and expected outcomes.

• Recognize project risks, develop contingency plans, mitigate issues, and keep clients informed.

• Set project quality benchmarks and inspire the team to commit to these standards.

• Manage client relationships at the study level and oversee client communications.

• Oversee project profitability, budgets, revenue recognition, forecasting, resources, pass-through costs, scope alterations, and invoicing.

• Coordinate cross-functional project teams to ensure successful study completion and client satisfaction.

• Represent Project Leadership in client meetings and presentations, including bid pursuits and investigator meetings.

• Engage in SOP reviews and contribute to other organizational initiatives.

⛳️ Requirements

• Bachelor’s degree or equivalent education (preferably in a Science or Medical field) or significant clinical project management experience.

• An advanced degree is preferred.

• Strong background in a CRO environment.

• Knowledge of Phase I, II-III clinical trial project management.

• Proven project leadership abilities.

• Extensive understanding of Oncology; familiarity with Ophthalmology, Neurology, Dermatology, or NASH is desirable.

• Proficient in written and spoken English.

• Strong skills in financial management and client relationship management.

• Experience with bid defense activities.

• Applications from candidates with pharmaceutical experience will also be welcomed.

• Knowledge of standard business and eClinical systems used in Clinical Research is advantageous.

• Familiarity with ICH and GCP regulations in relevant regions.

• Solid clinical knowledge and comprehension of clinical research and protocol design.

• Proficiency in Microsoft Excel, PowerPoint, Word, and project planning software.

• Ability to operate effectively in a matrix environment and independently with some oversight.

• Capacity to manage multiple priorities, organize workloads, and maintain meticulous attention to detail.

• Proactive, solutions-oriented mindset.

• Strong critical thinking and problem-solving abilities.

• Excellent interpersonal, verbal, and written communication skills.

• Strong client-oriented approach and accountability.

• Adaptable attitude towards tasks and learning opportunities.

🏝️ Benefits

• Competitive salary.

• Bonus opportunities.

• Car allowance (specific to the country).

• Comprehensive benefits package including holidays, pension, and other industry-leading benefits.

• Structured career progression and development within the role.

• Insight and understanding of the industry.