Clinical Project Manager, United Kingdom - L

Employer
CROMSOURCE
Location
United Kingdom
Salary
Competitive
Closing date
16 Oct 2020

View more

Discipline
Clinical Research, Clinical Project Manager
Hours
Full Time
Contract Type
Permanent
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Description:
Job Title: Clinical Project Manager

Location: Berkshire, United Kingdom

Schedule: Permanent or Freelance - Full Time

TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently recruiting for a Clinical Project Manager to join our client-based team. This is for one of the leading global biopharmaceutical companies, with a focus on Neurology and Immunology.

This is a permanent, office based position in the Berkshire area, with flexibility to work from home up to 3 days per week (while initially home based due to COVID). We can consider Freelancers but this role will fall within IR35.

The Clinical Project Manager will be working on Immunology trials and previous experience with Phase I studies is required.

Job specific tasks and responsibilities:
  • Delivery of one or more studies from protocol through to study report and archiving. These can be all types of studies from First in Human to Phase IV.
  • Manage the interface between the Sponsor, Phase I Unites, CROs and other vendors to ensure assigned studies are delivered according to contract specification, with high quality, on time and on budget.
  • Lead the internal and joint Clinical Study team, providing study-specific decision-making, developing strategies for increasing study efficiencies and co-coordinating issue detection, resolution and, where necessary, escalation to Program Delivery Leads.
  • Senior CPMs will be accountable for more complex studies and/or those with high visibility.


Education, Qualifications & Experience:
  • Bachelor's degree in a relevant field
  • Strong experience required in clinical development, including team leadership.
  • Experience managing in-house and/or outsourced regional or global Phase I, II and III studies (First in Human to multicenter clinical studies) from study start-up to study report completion.
  • Senior Clinical Project Managers must have substantial experience in study management in different indications and proven ability to manage complex multinational studies or multiple simultaneous studies from start to end.
  • Experience working with Immunology, or other complex therapies, such as Oncology, Rare Disease, Rheumatology, etc.


Skills & Knowledge:
  • Clinical trial management in Early and Late Phase and team leadership
  • Motivation, mentoring and integration of individuals on multi-functional international teams.
  • Delivery of scientific/medical presentations and training to both large and small audiences
  • Excellent verbal and written communication in English
  • Proficiency in the Microsoft Office suite
  • Good interpersonal skills
  • Excellent time management and organizational skills
  • Negotiation skills
  • Scientific and technical knowledge: GCP and regulatory environment; medical knowledge and research experience; and basic principles of data management and statistics
  • Proactive approach, drive and follow-through
  • Managing multiple concurrent responsibilities in an environment of changing priorities without close supervision
  • Ability to handle detailed technical matters and team dynamics
  • Reconciliation of conflicting priorities


Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Clinical Project Manager, Senior Clinical Project Manager, Project Manager, Clinical Study Manager, Study Manager, Phase I, Early Phase, Immunology, PM, CPM, SM, CSM, Pharmaceuticals, Pharma, Outsourced, Outsourcing, CRO, Contract Research Organization, Permanent

Skills: Clinical Project Manager, Immunology Location: United Kingdom Share:

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CROMSOURCE is an ISO-certified international provider of fully outsourced services to the pharmaceutical, biotechnology and medical device industries, specialised in clinical development and flexible resourcing solutions. CROMSOURCE was founded in 1997 and its successful growth has been built on stability, integrity, and high levels of customer satisfaction. We have grown steadily through offices across all regions of Europe and North America and delivering a comprehensive breadth of services.

Acting through PharmaceuticalMedical Device and Flexible Resourcing Solutions teams, and with a comprehensive portfolio of services, we offer a flexible approach to ensure CROMSOURCE optimally supports the unique needs of each client. This could mean providing regulatory consultancy to a small company at the early stages of a medical device development programme, through to provision of full services to a pharmaceutical company performing an international mega-trial to support registration of their product. Whatever the size and scope of the project, each receives the same level of attention to detail and commitment to delivery of a high quality service within budget and to timelines agreed.

We are experts providing experts and we live by our motto – Advise Agree Deliver. This means we leverage our experience and expertise at the early stages of discussions with our clients to freely advise them on the optimal project plan. We then reach agreement with each client on the scope of service, timelines and budget. CROMSOURCE then commit to deliver those services on time and within budget – according to our End-to-End Guarantee and this commitment to guaranteed delivery is unique in the clinical research environment.

Contact Us
  • 6-9 The Square
  • Stockley Park
  • Hayes
  • UB11 1FW
  • United Kingdom
  • +44 (0) 1786 468990
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