Local Clinical Trial Manager/Country Trial Manager - FSP

Job Overview

Parexel is seeking an experienced Local Clinical Trial Manager/Country Trial Manager in Germany. This role is fully remote and home-based.

Responsibilities

You will be accountable for the operational and scientific oversight, the set-up, execution, and delivery of assigned clinical trials at the local level. Your contributions will help deliver the pipeline through accurate planning and efficient execution of trials, bringing speed and value to participating patients and sites. You will provide leadership and direction to the wider trial team and be accountable for the overall success and delivery of assigned clinical trial(s) according to defined milestones and key performance indicators.

Key Duties:

• Oversee CRO and internal team activities to ensure trials comply with GCP-ICH, local/global regulations, application SOPs, and the trial protocol.
• Create, manage, and review trial budgets, ensuring appropriate financial oversight and planning accuracy, with timely updates based on trial changes.
• Ensure appropriate trial-specific training of internal and external partners is performed in line with the trial training plan.
• Accurately plan and coordinate operational feasibility of trial timelines and oversee trial preparation to ensure trial team members are aligned and on track.
• Verify and provide input into country and site-level feasibility and commitment. Finalize and validate site selection using available data sources and local insights/expertise, in collaboration with other functions.
• Develop and implement country-level engagement plans, recruitment planning, and risk mitigation strategies.
• Coordinate the development of country-level patient-facing documents in close collaboration with relevant internal and external stakeholders. Report patient and site-level feedback as strategic insight to improve trial design with a focus on patient value.
• Maintain oversight during clinical trial conduct, including adherence to GCP and all global and local regulatory requirements, compliance with SOPs, and continuous risk monitoring/mitigation. In collaboration with other functions, verify budget oversight, including support of regular clinical quality monitoring and safety reporting.

About Parexel

Parexel supports clinical studies across a wide range of therapeutic areas and has longstanding partnerships with a vast client base. We have supported trials for many of today's top-selling drugs, as well as niche drug developments critical to patient well-being. You'll be an influential member of the wider team.

Qualifications

• Minimum of 5 years of relevant clinical trial management experience.
• Experience managing outsourced trials or CRO Management.
• Vendor Management experience.
• Excellent leadership, communication, and organizational skills.
• Ability to multitask under limited direction and on own initiative.
• M.S/M.A/Ph.D or B.A/B.S/nursing degree is essential.

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EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.