Skip to main content

This job has expired

Clinical Research Manager - P

Employer
ClinChoice
Location
United Kingdom
Salary
Competitive
Start date
26 Mar 2019
Closing date
25 Apr 2019

View more

Discipline
Clinical Research
Hours
Part Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Description:
Job Title: Clinical Research Manager

Location: United Kingdom

Schedule: Full time, 37.5 hours per week

For our client-facing positions, you must be confident, be able to drive the role and work autonomously. You will have a close relationship with our Line Managers, who will provide you with mentoring and guidance. Most of our roles are permanent positions with CROMSOURCE and you will be working on studies for just one client. We are open, friendly and approachable and aim to support you through the recruitment process every step of the way.

TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently recruiting for a Clinical Research Manager for one of our clients based in France. We are flexible with the working location, either home-based or office based at our office in Stirling. This job requires you to be flexible when it comes to traveling to France.

Essential Function:

The Clinical Research Manager is responsible for assuring the co-ordination of the operational aspects and proper conduct of a clinical study, including compliance with International Conference on Harmonisation (ICH) Harmonised Tripartite Guideline for Good Clinical Practice (GCP) and Client policies and standard operating procedures.

Key Accountabilities:
  • With some oversight, will co-lead and manage the implementation of assigned studies.
  • Accountable to ensure all relevant studies follow SOPs & GCP.
  • Leads the matrix team with key study partners (e.g. Regulatory, Compliance, Clinical Supplies).
  • Maintain relationships and monitor performance of CROs & other vendors for contracted studies.
  • Track timelines and identify contingencies and risk planning to meet overall timeline goals.
  • With oversight, develop study timelines and study implementation plans.
  • Manage study start-up, conduct, & close-out.
  • Manage clinical trial material and assist in forecasting.
  • Assist with operational feasibility in study design.
  • Ensure Ethics and Health Authority submissions are completed on time.
  • Ensure timely delivery of database freeze/authorised database.
  • Developing content and driving execution of investigator meetings/will present selected topics.
  • Provide significant input into development of CRF such that the final version is influenced.
  • Manage study start up and ensure patient recruitment plans are in place.
  • Coordinate input into informed consent form.
  • Serve as single point of contact for country/site questions relating to study operation issues; liaise with appropriate study team members as needed.
  • Contribute to status reports for program reviews and senior management.
  • Participate in key organisational process improvement initiatives


Education, Qualification & Experience:
  • Educated to degree level (biological sciences, pharmacy or other health related discipline preferred).
  • Substantial experience in Clinical Research including previous Clinical Research Manager experience.


Skills:
  • Excellent verbal and written communication skills and organisational and team leadership skills.
  • Client focused
  • A flexible attitude with respect to work assignments and new learning.
  • Ability to effectively and proactively manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
  • Willingness to work in a matrix environment and to value the importance of teamwork
  • Possess strong negotiation, diplomacy, team leadership skills and excellent organisational ability.
  • Ability to motivate both individually and collectively.
  • Excellent problem solving capability through early identification.
  • Demonstrate, appreciation and understanding of finance and budgeting issues.
  • Accountability for all designated tasks.
  • Excellent computer literacy.
  • Competent in written and oral English.


If you have the experience needed for this position, please apply directly to https://www.talentsourcelifesciences.com/job-information/?job-id=Hq00001709 . If you would like to discuss the role before applying through the website, please contact Laura.Guascone@cromsource.com for more information.

Benefits working for TalentSource
  • Dedicated Line Manager
  • Monthly meetings with line manager
  • Employee satisfaction survey - your feedback is important for continuous improvement
  • Annual appraisals development planning
  • Yearly team event
  • New Year's diner
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally


Why choose TalentSource Life Sciences/CROMSOURCE?

TalentSource Life Sciences is a fully dedicated flexible resourcing department at CROMSOURCE, a family owned international, full-service Contract Research Organisation. CROMSOURCE comes from the merger of MSOURCE and CROM and we have been supporting clients with outstanding clinical research and resourcing services since 1994. Successful growth has been achieved by putting high quality and client focus at the heart of everything we do and we are proud to partner with industry leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide.

Our employees are the most valuable company asset and because we want to retain our staff, we ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all 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 clear tools to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our current below industry average turnover rates.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are experts providing experts - highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world.

Key words: Clinical Research Manager, Clinical Project Manager, Clinical Study Manager, Project Manager, Study Manager, PM, SM, Clinical, Outsourced, Permanent, CRO, Contract Research Organisation, Pharma, Pharmaceutical
Skills: Clinical Project Manager, Clinical Research Manager, Clinical Study Manager Location: United Kingdom

Company

ClinChoice

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

 

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

 

Company info
Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert