Precision Medicine Group

CRO

(Senior)ProjectManager

Remote (Poland) Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“(Senior) Project Manager at Precision Medicine Group. Skills: Project Management, Clinical Trials, Oncology, CRO. Lead clinical projects. Manage study budget and scope”

What You'll Achieve.

ensuring agreed timelines, scope, cost and quality; achieve objectives in the execution of contracted objectives; achieve financial objectives

Industry & Context.

CRO
Eligibility Requirements

Availability for domestic and international travel including overnight stays

What They're Looking For.

Must Have

Previous experience in a full service/global Project Management role working in the CRO industry is essential, at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation, 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, presentation skills, Proven computer skills (MS Office, MS Project, PowerPoint), software experience (CTMS, eTMF, EDC, IXRS), Proven ability to develop positive working relationships with individual 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

Nice to Have

experience in Oncology

What You'll Do.

Lead clinical projects

Manage study budget and scope

Set and achieve objectives

Run international trials

Serve as primary point-of-contact liaison with client

Provide excellent customer service

Participate in proposal activities

Participate in client presentations

Liaise with Project Team and senior management

Handle all aspects of clinical research trial

Manage all functional areas

Prepare project status updates

Identify key deliverables and performance metrics

Contribute towards efficient management and execution of trials

Prepare and reviews protocols

Prepare and reviews study documentation

How You'll Work.

Team & Collaboration

Work in a cross-functional team with internal and external stakeholders; Coordinate the study team; Develop positive working relationships with individuals and teams internally and externally

Communication Scope

communicate effectively in English; presentation skills

Process & Methodology

full service oversight for clinical projects, oversight of all functional departments, ensuring agreed timelines, scope, cost and quality, managing the client relationship, project team and budget and timelines, clinical project delivery, project execution, financial objectives management

Full Job Description

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 are looking to hire a (Senior) Project Manager with experience in Oncology who have 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 global/regional (ph 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. We offer an amazing high-energy, dedicated, collaborative team 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 exce

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