Company

KCR

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Project Manager (IS)

City/voivodeship

Israel

Publication

2018-12-19

Company description

KCR is a contract research organization providing clinical development solutions for the pharmaceutical, biotechnology and medical device industries.
The company supports clients with full-service capabilities across three main services: Trial Execution (TE), Functional Service Provision (FS) and Trial Execution Consulting (TC) over a broad range of therapeutic areas. 
KCR operates across four main regions: North America, Western Europe, Central Europe, and Eastern Europe with hubs located in Boston, U.S., Berlin, Germany, Warsaw, Poland and Kiev, Ukraine. KCR’s geographical locations allow for optimized delivery of trial execution strategies to develop life-changing therapies. For more information visit www.kcrcro.com.
KCR: We see human behind every number
A leading Clinical Research Organisation (CRO), with over 20 years of presence on the international market, operating across 27 countries is seeking to employ experienced Project Manager.
The new incumbent shall take full accountability for international project and study program delivery on time, with quality and within planned budget.
Location:  Israel (home-based)

The duties associated with the role include:
  • Controlling realization of the clinical research study at all stages.
  • Ensuring that assigned projects are delivered on time, within budget and with quality.
  • Proactively reporting study progress, delays and risk, as well as associated action plans.
  • Preparing reports on the assigned activities according to the requirements, timelines and realization of study budget.
  • Taking part in teleconferences and meetings with Sponsor, services providers and team members from other departments
  • Participating in sponsor audits and Regulatory Authority inspections
  • Cooperating actively on preparation and conduct of Bid Defense Meetings organized by B&D Department when requested.
  • Managing contracting and coordinating work of all services providers
  • Supervising accurate reporting of study costs by services provider.
Requirements:
  • University degree in life sciences or equivalent clinical research experience
  • At least 5 years clinical research experience including 3-4 years project management responsibility for international study
  • Excellent understanding of the drug development process
  • In depth knowledge of applicable clinical research regulatory requirements; i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Focused on project work, driving results based on set milestones, assuring compliance with applicable regulations and work schedules
  • Proven ability to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback and coaching
  • Strong understanding of, and experience managing, contractual obligations and implications
  • Excellent communication and negotiation/influencing skills
  • Flexibility to work with different time zones
At KCR we put our mission: WE SEE HUMAN BEHIND EVERY NUMBER into our actions, therefore we offer our Employees benefits
that comply with national regulations and provide the coverage that best meets employee needs.
To show that you are appreciated in our team, while working at KCR you will be provided with: 
  •  3-step onboarding process to enable you fast takeover of duties
  •  Peer Buddy Mentor who will introduce you to the organization
  •  Friendly office space, coffee, tea and sweets
  •  Flexible, remote working options
  •  Time off – additional days of holidays for birthday, leaves of absence
  •  Loyalty bonus for long term cooperation
  •  Employee referral program
  •  Empowering workspace, offering opportunities to share ideas and influence company services development worldwide
  •  Open culture based on our values: knowledge, customer focus, accountability, commitment, tenacity and determination to succeed
  •  Mentoring and training programs related with clinical trials, therapeutic areas, soft skills development
If you wish to apply, please submit your CV using the button below.