Senior Clinical Project Manager

Precision Medicine Group; United Kingdom; On-site; GBP 70,000 - 90,000; Full time

Job summary

A global clinical research organization is seeking a Senior Project Manager to oversee clinical trials, particularly in Oncology. The role requires extensive experience in project management within the CRO industry, strong interpersonal skills, and a proven ability to manage international trials. This position offers a dynamic work environment with a focus on delivering high-quality outcomes for patients. Competitive compensation and opportunities for growth are included.

Benefits

Collaborative work environment

Work-life balance support

Career growth opportunities

Qualifications

• 5-7 years of industry experience in clinical trials.
• At least 3 years in full-service project management.
• Experience managing studies within Oncology.

Responsibilities

• Lead clinical projects in accordance with the study budget.
• Serve as the primary point-of-contact for clients.
• Prepare project status updates and performance metrics.

Skills

Project management

Client liaison

Interpersonal skills

Organizational skills

Presentation skills

Education

Degree in life sciences or equivalent

Tools

MS Office

MS Project

CTMS

eTMF

EDC

IXRS

Job description

Overview

Are you an experienced full service Project Manager in the field of clinical trials who can address 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 and prove 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 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 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 you will see 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 a high-energy, dedicated, collaborative environment with team members who enjoy a challenge, thrive in the details and flourish in dynamic environments. If you are ready to take charge and seek positive teamwork to deliver extraordinary work, this is 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
• 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 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 a genuine passion for rare diseases and oncology.

We are a people-focused CRO with a supportive and collaborative environment that promotes work-life balance and encourages team development.

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

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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 [e-mail].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.