Senior Clinical Project Manager

Discipline: Clinical Research
Job type: Permanent
Salary: £$135,000 - $150,000
Contact name: Joe Pearce

Contact email:
Contact phone: +44 1293 584 300
Job ref: 24446
Published: 5 days ago
Expiry date: 02 Sep 2022 11:59

Senior CPM / Decentralized Clinical Trials / DCT CRO / Remote / Multiple Therapeutic Areas / $135k - $150k plus package & benefits


RBW Consulting are excited to announce an opportunity on behalf of one of our close clients. This company are a specialist decentralized clinical trial (DCT) CRO that offer hybrid clinical research solutions through its technology platforms and medical services. Regarding decentralized approaches in clinical research, the Senior CPM will be breaking ground into new spaces that no other CROs or companies are doing at this time. This includes direct to patient site services, sample logistics, study oversight, labs, devices, data collection, and much more. The clinical operations department at this company is projected to grow by 50%-75% per year for the next several years and the company itself already have 400+ employees worldwide. This means you will have the space and opportunity to grow; potentially stepping into a strategic or leadership role in the near future as the company progresses.


This company is running several trials at the moment in the areas of CNS, General Medicines, Infectious Diseases, Women’s Health, and Device/Diagnostics. The Senior CPM will be typically assigned to 2-3 clients at a time and will report into the VP of Clinical Operations. During the onboarding period, you will receive company and functional training as well as project support training per study as assigned by director-level staff. Due to their continued growth, my client seek a project manager with sufficient knowledge of project management fundamentals, project scope, project timelines, quality & risk assessment, and resource management. The Senior CPM will be accountable for operational oversight and reporting, project finance acumen, knowledge of clinical trial & operational process, protocol comprehension, strong leadership and knowledge of rules & regulations.


This is a great opportunity to join a company that is on the up, in an environment that is fully flexible and transparent at all levels. You will have the opportunity to be an integral part of growing a unique company that is tackling decentralized clinical trials in the right manner. Not only will you have the chance to engage directly with the VP of Operations and other Senior-level staff regularly, but you can wear many hats and develop your overall skillset individually, as well. As the company expands in North America and soon into Europe, you will be at the forefront of the company’s success and will be able to impact their success, worldwide. With that comes a handful of opportunities to stimulate your own growth and professional development.


Duties include but are not limited to:

  • PM services including (but not limited to), budget, resourcing, client management, quality control, training, mentoring, SME, and process improvement.
  • Will demonstrate global PM experience as well as successful application of risk evaluation methods.
  • Delivering project objectives on time and on budget
  • Executing clinical trials end-to-end to ensure effective and timely internal and external communication of study progress, issues, and plans for resolution
  • Provides an intuitive approach in managing client and external stakeholder expectations in the subjects of risks, expenditure, quality, and timing
  • Guides/trains other staff members in clinical operations team or functional leads, as required
  • Comfortable aiding in business development endeavours to win new client bases and actively seeks strategic opportunities from initial engagement
  • Confident developing and delivering presentations and engaging with prospective/existing clients


Qualifications & Skills

  • Bachelor’s degree or equivalent required
  • 5+ years of relevant experience within clinical research
  • At least 1+ year of industry project management experience within pharmaceutical, biopharmaceutical, or contract research organisation (CRO) environment
  • Drug development experience in interventional or observational trials
  • DCT experience preferred but not required
  • Multiple therapeutic backgrounds welcome



  • 0% travel
  • Fully remote working
  • Full paid-time-off (PTO)
  • Family-like culture
  • Varied responsibilities
  • Unhindered professional growth opportunities
  • Transparent business
  • Unique technology and medical services


To apply:

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 1273 049 215 or email me at


Please click ‘apply’ or contact Joe Pearce for any further information


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RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status.