Clinical Trial Manager / pan-European studies / Hampshire / UK

Employer
DOCS Global
Location
Hampshire, UK
Salary
Competitive
Closing date
24 Sep 2020

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Discipline
Clinical Research, Clinical Trials Manager / Administrator
Hours
Full Time
Contract Type
Permanent
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We are looking for Clinical Trial Managers with experience of leading/managing pan-European studies within a CRO, pharma or biotech work setting.

Key responsibilities stop include:

• Lead and manage the conduct of clinical trials from study start-up to close-out across multiple countries in accordance with ICH-GCP and applicable local regulations
• Collaborate with Clinical Trial Managers (and the Global Clinical Trial Manager for global execution of study(ies)
• Maintain the quality and scientific integrity of clinical trials across multiple countries
• Collaborate with cross-functional internal and external stakeholders to ensure timely and on budget execution of clinical trial deliverables within multiple countries

Key Responsibilities include:
• Identifying and resolving issues at a regional level
• Collaborating with Global Clinical Trial Manager(s) to ensure country level study delivery is aligned with the global study project plan
• Contributing to study-level risk assessments
• Leading and continually review regional risk mitigation activities to ensure study delivery to plan
• Overseeing regional insourcing/outsourcing partner deliverables to the required standards
• Ensuring regional, country and site vendor set-up, conduct and quality e.g. laboratories and equipment provisioning
• Leading regional documentation and required tool and systems set-up
• Contributing to regional aspects of Drug Supply Plan
• Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines
• Supporting audit and inspection activities and contribute to CAPAs, including leading resolution of issues when appropriate
• Executing regulatory agency inspection readiness activities (e.g. TMF review, story board generation) within region
• Supporting and contributing to Clinical Study Team(s)
• Ensuring relevant systems are updated to enable accurate reporting of study progress and milestone deliverables
• Ensuring key stakeholders are kept informed of study progress e.g. Global Clinical Trial Managers, etc.
• Contributing to development of study-specific materials e.g. monitoring plan, study specific training documents
• Participation in cross-functional task forces / process improvement groups

Critical Success Factors for the Role include:
• Working knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP), and applicable international regulations and guidelines
• Clinical Development process and procedures
• Project planning experience including oversight of study deliverables, budgets, and timelines
• Ability to use scientific and clinical knowledge to conceptualize study designs
• Experience anticipating and resolving problems
• Experience writing and presenting clearly on scientific and clinical issues
• Experience collaborating and leading cross-functional teams (team/matrix environment)
• Knowledge of project risk management assessment and mitigation approaches

What is required
• BA/BS/BSc in the sciences or RN
• Ideally, a minimum of 7 years work experience in life sciences or medically related field, with ideally at least 4 years clinical research experience obtained working on clinical trials either within a biotech, pharmaceutical or CRO company
• Proven track-record of European clinical studies (commercial/industry-sponsored studies)
• Experience in working with external clinical research vendors (CROs, central labs, imaging vendors, etc.)
• Full and valid UK working eligibility
• Ideally able to start asap/negotiable

What is offered
• Permanent contract of employment with DOCS seconded to the client;
• Full-time;
• Office-based at Eastleigh (Hampshire/UK) - 3 days in the office and 2 days home-working;
• Competitive salary depending on level of skills and experience;
• Company benefits: 25 days annual leave plus UK bank holidays, car allowance, pension and healthcare.

Why Join DOCS?

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

If you are an experienced clinical study/clinical trial manager, contact me now for more details with your latest CV* at Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

*Applicants who have not had a response within two weeks should assume their application has been unsuccessful.

#PMjob

DOCS provides global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry. 

 

Our Values

At DOCS, we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are:

OUR PEOPLE: We attract, source, develop and retain the best talent to enables us provide world-class people and solutions for our clients.

EXCELLENCE: We never stop looking for new, better ways of working.

ACCOUNTABILITY: We take responsibility for our actions, owning our client’s problems and proactively looking for solutions.

INTEGRITY: Becoming a trusted partner means being honest, respectful and ethically sound, at all times.

OPENNESS: We encourage and facilitate an open and inclusive environment for a diverse global network of employees and stakeholders.

Contact Us
  • 2 Globeside
  • Globeside Business park
  • SL7 1HZ
  • United Kingdom
  • +44 (0) 2380 688500
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