Company

KCR

Advertisement

Senior Clinical Research Associate (US / Southwest)

Publication

2021-04-28

Company description

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 now operates across five regions: North America, Western Europe, Central Europe, Eastern Europe, and Australia, 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 the 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.

Senior Clinical Research Associate / CRA II

 
Location:  US / South West region (home-based)
 

To our fast growing US team,  we seek for an experienced Clinical Research Associate to be involved in interesting projects across East Coast of the US and shape future of pharmaceutical therapies.

 

The duties associated with the role include:

  • Performing site visits and monitoring activities in accordance with protocol, GCP/ICH 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
  • ​Leading, coaching and mentoring CRAs team to assist in their development and training
  • Responsible for execution of KPI`s for assigned staff and for all site deliverables within required time and budget
  • Providing leadership for the development and implementation of new training programs and improvement of current programs for assigned staff

 

Requirements:

  • University degree in life sciences/pharmacy/biotechnology
  • At least 2-3 years of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines
  • Proven experience with line management
  • Deep knowledge of monitoring procedures and entire clinical trial process
  • Computer competency
  • Fluent command of English
  • Ability to complete tasks in an accurate and timely manner

 

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 career in clinical trials industry
  • Onboarding process to enable you fast takeover of responsibilities
  • 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
  • 33 PTO days + 1 additional day for Birthday
  • Attractive healthcare benefits
  • 401k on a level of 3%
  • Life, long & short-term disability and international travel insurance
  • Discounts program
 
If you wish to apply, please submit your CV using the button below.
*please note you need to have current right to work in US to apply