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Overview

Are you an experienced full service Project Manager in the field of clinical trials focused on Oncology? Precision for Medicine (CRO) is 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. You will have full service oversight for clinical projects across global/regional (Phase 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 timelines, scope, cost and quality are met. You will be involved in all study stages, including proposal strategy, development, costing, 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 internal and external stakeholders, driving quality and coordinating the study team.

We offer a high-energy, collaborative team environment. If you are used to taking charge and seek positive teamwork to deliver excellent work, we have an opportunity for you.

Responsibilities

• You will independently lead clinical projects in accordance with the study budget and scope of work, using strong interpersonal and organizational skills to set and achieve objectives for both contracted 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 the Project Team and senior management of both Precision and sponsors, including C‑level executives.
• Handle and lead all aspects of a clinical research trial or trials.
• Provide 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, and manage escalation when needed.
• Serve as an active member of the Project Team with the goal of contributing to efficient management and execution of trials.
• Prepare and review protocols and other study documentation such as project plans, informed consents, site contracts and budgets.

Qualifications

• Degree or related life science qualification, or equivalent combination of education and experience.
• Previous experience in a full-service/global Project Management role in the CRO industry is essential.
• 5 to 7 years of industry experience and at least 4 years of full-service Project Management experience in a clinical trial setting, working for a CRO.
• Experience managing studies within Oncology.
• Working understanding of GCP/ICH guidelines and the clinical development process.
• Ability to travel domestically and internationally, including overnight stays.
• Proficiency in English (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 they relate to the execution of a clinical development plan.

About Precision for Medicine

Precision for Medicines 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 a passion for rare diseases and oncology. We are a people-focused CRO with a supportive and collaborative environment that promotes work-life balance and team development.

We invite you to learn more about our growing organization serving clients researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for their contributions every day.

Legal and Privacy

Any data provided as part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please refer to our CA Privacy Notice. 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. If you require a reasonable accommodation to complete any part of the application process or need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.

It is important to note that some individuals or organizations may pose as potential employers offering enticing employment opportunities. These offers are not associated with our company and may be fraudulent. We will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.