Precision Medicine Group
Clinical Project Manager / Senior Clinical Project Manager
Remote work allowed only within certain countries or regions.
Employer listed it 2 days ago · Found 9h ago
First listed 2 days ago.
Salary
Not stated
Location
Timezone
Not stated
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
Region Restricted
Remote work is allowed, but only for candidates based in Slovakia, United Kingdom.
What the employer says
- Source listing states candidate location: "Remote, Slovakia, Remote (UK)"
What Nomaders makes of it
- Applications outside the listed area are usually rejected
- Timezone overlap with the listed area is often expected
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
- 1Check the flexibility label above, region restricted, matches where you plan to live and work.
- 2Tailor your CV to the role at Precision Medicine Group, mentioning your remote working experience.
- 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.
Similar roles
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