Are you an experienced full-service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology. Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?

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Precision for Medicine are looking to hire a (Senior) Project Manager with experience in Oncology who has managed full-service clinical trials within a CRO setting to join our global team.
In this pivotal role you will have full-service oversight for clinical projects across integral/regional (phase I-IV) trials, within Oncology. Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.
Involved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.
You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team.
How we will keep you busy and support your growth

You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well.
Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations




Liaise with Project Team and senior management of both Precision and sponsors, including C level
Handle and lead all aspects of a clinical research trial or trials
Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.
Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials
Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets
Requirements

Degree or similar related life science qualification, or equivalent combination of education and experience.
Previous experience in a full-service/global Project Management role working in the CRO industry is essential.
5 to 7 years industry experience and at least 4 years full-service Project Management experience in a clinical trial setting working for a Clinical Research Organisation. xqbhyrx

Experience managing studies within Oncology
Working understanding of GCP/ICH guidelines and the clinical development process

Ability to drive and availability for domestic and international travel including overnight stays
Be able to communicate effectively in the English language both written and spoken
Strong presentation skills
Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)
Proven ability to develop positive working relationships with individuals and teams internally and externally
Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

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📌 Clinical Project Manager (Madrid)
🏢 Precisionmedicinegroup
📍 Madrid