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Precision Medicine Group

Clinical Project Manager / Senior Clinical Project Manager

Work from homeNew this week

Remote role where the employee must remain based in a particular country.

United Kingdom only

Employer listed it 2 days ago · Found 9h ago

First listed 2 days ago.

Salary

Not stated

Location

United Kingdom only

Timezone

GMT

Contract

Full-time

Experience

Senior

Category

Operations

This employer didn't state pay. Jobs like this usually pay around $105k–$180k a year, a typical range taken from 186 senior-level operations roles on Nomaders that do state pay. It's a guide, not an offer.

Remote flexibility

Work from home

This is a remote role, but the employee must be based in United Kingdom. It is work from home rather than work from anywhere.

What the employer says

  • Source listing states candidate location: "Remote, United Kingdom, Remote (UK)"

What Nomaders makes of it

  • Residency required in United Kingdom
  • Payroll and tax are likely handled in that country only

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

About the role

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

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

Benefits

No benefits package published with this listing. Ask about it at first interview.

How to apply

  1. 1Check the flexibility label above, work from home, matches where you plan to live and work.
  2. 2Tailor your CV to the role at Precision Medicine Group, mentioning your remote working experience and working hours (GMT).
  3. 3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 9h ago. Last checked 23 Sept. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.

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