Senior Clinical Project Manager, Internal Medicine (Home-based, UK/Europe) - IQVIA Biotech (R1085826) in Stevenage, UK bei IQVIA™

Datum der Veröffentlichung 4/6/2020


  • Mitarbeiterkategorie:
  • Standort:
    Stevenage, UK
  • Berufserfahrung:
    Not Specified
  • Datum der Veröffentlichung
  • Job ID:


IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.


Responsible for all activities related to implementation of clinical studies including:

•    Manages projects of full scope regional and global projects.  Responsible for project team leadership
•    Responsible for building and maintaining positive  client relationships
•    Ability to negotiate with clients to assure Novella’s operational processes are maintained, projects are done within scope
•    Reviewing and identifying project study trends and proactively responding to client and respective team members
•    Developing appropriate early warning systems of potential obstacles to the successful completion of the projects; analyzes information and develops innovative solutions to challenges
•    Identifying, define, document  training requirements in LMS systems and assure project level compliance with study specific training requirements
•    Responsible for change management on all assigned projects
•    Responsible for assuring projects assigned are run according to SOPs and WP as refined in the contract
•    Responsible for assuring project timelines are met as per contract
•    Responsible for identifying processes which need updating and documenting that to the direct line manager or divisional lead
•    Responsible for maintaining client relationships for all assigned work, keeping all project reporting current, and assuring executive management is aware 
•    In conjunction with management, assists with developing, documenting, and updating internal processes and processes required for consistency across programs such as SOPs, working practices, and related quality assurance forms.
•    Provide other project support to Managers, as assigned
•    Oversee delegation of support staff activities, as necessary
•    Assists in the development and delivery of capability and proposal defense presentations to prospective clients
•    Supports Contracts and Proposals with final project contract execution and CIS documentation by the project team.  Represents senior management in negotiation of contracts as appropriate.
•    Participates in the performance appraisal program by providing timely and accurate feedback regarding the performance of respective team members at least annually
•    Maintains current knowledge of FDA regulations, and GCP and ICH Guidelines for clinical research.
•    Responsible to maintain personal currency documentation for Novella SOPs, CAPA completion and timesheet maintenance including assurance or back-up PM staff at each and every instance of out of office


•    Thorough knowledge of clinical research process from Phase I through regulatory submission
•    Strong communication skills (verbal and written) to express complex ideas
•    Excellent and demonstrated organizational and interpersonal skills
•    Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities
•    Ability to manage multiple priorities within a variety of complex clinical trials
•    Ability to reason independently for the purpose of assessing and recommending specific solutions in clinical settings
•    Ability to set baseline targets, track trends and implement mitigation plans
•    Understanding of basic data processing functions, including electronic data capture
•    Demonstrated problem-solving and financial negotiation skills  
•    Working knowledge of current ICH GCP guidelines

•    Previous Management Requirements:
    Nursing or University degree (US Bachelor Level or equivalent) in a health-related field with at least five (5) years direct clinical trial experience in a CRO or research-related organization with at least two (2) years management experience OR 
    Equivalent level of education and experience.  
    Previous experience in managing people within a scientific/clinical environment is required. 
•    Demonstrated Clinical Monitoring and/or Data Management experience required.  
•    Excellent verbal and written communication and presentation skills required. 
•    Demonstrated financial management skills required
•    Ability to work independently, prioritize and work with in a matrix team environment is essential.  
•    Working knowledge of Word, Excel, and PowerPoint required.  
•    Prior experience in electronic data capture preferred.  
•    Ability to travel domestically or internationally as required.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1085826