Company

KCR

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Clinical Research Associate (PL)

Publication

2021-01-08

Company description

KCR is a clinical development solutions provider for the biotechnology, pharmaceutical, and medical device industries. We support clients with full-service clinical development capabilities across three main areas: Trial Execution, Consulting and Placement. KCR operates across four main regions: North America, Western Europe, Central Europe, and Eastern Europe, with a main operational hub located in Boston, MA. Our strategic hub locations, technical capabilities and solution offerings allow for the optimized delivery of trial execution strategies to develop life-changing therapies. KCR offers access to an estimated population of 1.1 Billion people. For more information visit www.kcrcro.com.
KCR: We see human behind every number

KCR is a clinical development solutions provider for the biotechnology and pharmaceutical industries. We support clients with full-service clinical development capabilities across three main areas: Trial Execution, Consulting and Placement. KCR operates across four regions: North America, Western Europe, Central Europe, and Eastern Europe, with a main operational hub located in Boston, MA. Our strategic hub locations, technical capabilities and solution offerings allow for the optimized delivery of trial execution strategies to develop life-changing therapies. KCR offers access to an estimated population of 1.1 Billion people. For more information visit www.kcrcro.com. We see human behind every number.

 

Clinical Research Associate

Location: Poland (home-based)


Responsibilities:

  • Performing feasibility activities, site visits and monitoring activities in accordance with protocol, ICH-GCP Guidelines and other applicable requirements
  • Ensuring overall integrity of study and adherence to guidelines, protocol and regulations
  • Taking an active role in the project team by providing feedback and suggestions for successful completion of the project
  • ​Coaching and mentoring less experienced CRAs to assist in their development and training

Requirements:

  • University degree in life sciences/pharmacy/biotechnology or related field
  • ​Years of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, ICH-GCP Guidelines:
  • CRA I Level: min. 1 year
  • CRA II Level: min. 2 years
  • Senior CRA Level: min. 3 years
  • Very good written and oral communication skills
  • Ability to manage multiple priorities
  • Good organizational and time management skills
  • Strategic thinking: ability to anticipate potential issues and take appropriate actions
  • Ability to work in a team or independently as required
  • Highly motivated with proactive approach
  • Computer competency
  • Fluent command of English and Polish
  • Valid Driver's License cat. B
  • Ability to travel
  • Oncology or/and phase I experience will be an asset

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:

  • Ability to join international CRO company and develop knowledge of clinical trials industry
  • Possibility of getting involved in multinational studies 
  • Onboarding process to enable you fast takeover of duties
  • Peer Buddy Mentor who will introduce you to the organization
  • Flexible, remote working options
  • Open culture based on our values: learning, customer focus, accountability, commitment, tenacity and determination to succeed
  • Empowering workspace, offering opportunities to share ideas
  • Mentoring and training programs related to clinical trials, therapeutic areas, soft skills development 
  • Sport card, healthcare coverage, additional benefits cafeteria, NNW insurance, additional days-off for certain occasions