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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?
Precision for Medicine (CRO) is looking to hire a Senior Project Manager ideally with experience in Oncology & either CAR T or Radio Pharm who has managed full service clinical trials within a CRO setting to join our global team.
We can consider candidates living in the following countries: Poland, Hungary, Romania, Slovakia, Serbia, UK or Spain.
In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost, and quality.
You will be 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, 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.
Precision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.
We are a people-focused CRO with a supportive and collaborative environment which promotes work-life balance and encourages team development.
We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.
We offer an amazing high-energy, dedicated, collaborative team of members who enjoy a challenge, thrive in the details, and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.
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 3 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
Experience managing studies within Oncology with additional experience in Radio Pharm and/or CAR T.
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.
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