Company

KCR

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Internship in KCR Regulatory Affairs Department

Publication

2021-09-14

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 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.comWe see the human behind every number

 

 
Internship in KCR Regulatory Affairs Department
 
3-month internship with possibility to extend the contract
 
Location: Ukraine
 

Would you like to get into the clinical research industry?

 

At KCR we are always looking for new talents to join our dedicated team of professionals!

 

Join us and support our Regulatory Affairs team in realization of all aspects of clinical study registration to Competent Authorities and Ethics Committees in assigned countries according to Standard Operating Procedures (SOPs), GCPs, ICH guidelines and local laws and regulations.

 

Your profile:

4th / 5th year student or graduate, preferably of life sciences studies;

- Previous experience in a similar role / industry would be an advantage;

- Understanding of common administrative work rules, document management and preparation as well as contact with applicable authorities;

- Knowledge of MS Office;

- Fluent English.

 

Our offer:

- 3-month internship with possibility to extend the contract;

- Ability to join fast-growing international CRO company and develop knowledge of clinical trials industry;

- Open culture based on our values: knowledge, customer focus, accountability, commitment, tenacity, and determination to succeed;

- Empowering workspace, offering opportunities to share ideas and influence company services development worldwide.