Precision for Medicine

Global CRO for precision medicine trials

Senior Clinical Project Manager - Oncology

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeRemote in UKNo salary listed

About the Job

Requirements

A degree or similar related life science qualification, or an equivalent combination of education and experience, is required.
Previous experience in a full-service/global project management role in the contract research organization industry is essential.
Extensive experience in a clinical operations position within a contract research organization is required, including at least four years of full-service project management experience in a clinical trial setting at a clinical research organization.
Experience managing oncology studies is required.
A working understanding of Good Clinical Practice and International Council for Harmonisation guidelines and the clinical development process is required.
A valid ability to drive and availability for domestic and international travel, including overnight stays, are required.
Effective written and spoken English communication is required.
Strong presentation skills are required.
Computer skills with Microsoft Office, Microsoft Project, and PowerPoint, and experience with clinical trial management systems, electronic trial master files, electronic data capture, and interactive voice/web response systems, are required.
The ability to develop positive working relationships with individuals and teams internally and externally is required.
A core understanding of medical terminology and clinical trial activities as they relate to execution of a clinical development plan is required.
Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsibilities

Independently lead clinical projects in accordance with the study budget and scope of work, setting and achieving contracted and financial objectives; this may include running international trials.
Serve as the primary client liaison, providing customer service and participating in proposal activities and client presentations.
Liaise with project teams and senior management at Precision and sponsor organizations, including C-level executives.
Handle and lead all aspects of one or more clinical research trials.
Manage projects across functional areas, including data management, safety, clinical, medical monitoring, and biostatistics.
Prepare project status updates for clients and management, identifying key deliverables, performance metrics, and matters requiring escalation.
Actively contribute as a project team member to efficient trial management and execution.
Prepare and review protocols and other study documentation, including project plans, informed consents, site contracts, and budgets.
Provide full-service oversight for global and regional Phase I–IV oncology trials, with accountability for clinical project delivery, functional department oversight, and agreed timelines, scope, cost, and quality.
Participate in study proposal strategy, development, costing, and bid defense, and manage studies through completion, including client relationships, project teams, budgets, and timelines.
Coordinate internal and external stakeholders and the study team to drive quality.

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 Clinical Project Manager / Senior Clinical 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 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 reviews protocols and other study documentation such as project plans, inform 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.
Extensive experience working within Clinical Operations position within a CRO, and 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
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 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

Precision for Medicine's 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 focussed 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.

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also 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 are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Candidates must be legally authorized to work in the country of employment without employer sponsorship.

About the Company

Precision for Medicine

Global CRO for precision medicine trials

Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company size: 1,001-5,000
Company stage: Growth Equity (Venture Capital)
Total funding: $225M
Headquarters: Bethesda, MD
Founded: 2012

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