Clinical Trials Associate (Serbia)

Location: Belgrade, Central Serbia, Serbia

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Requisition Number: 1570

Position Title: Clinical Trials Associate

External Description:

The Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

 

RESPONSIBILITIES:

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
  • Maintain and quality audit to assure the most recent revisions of documents are on project portals
  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
  • Maintain version and quality control of project documentation and submit to trial master file
  • Assist with the tracking and maintenance of project related information, including site medical question and answer log
  • Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
  • Maintain current participating site and personnel information
  • Arrange and track the distribution of project specific training to the project team

 SKILLS AND ABILITIES:

  • Excellent written and verbal English as well as fluency of the language of the country of location
  • Strong interpersonal skills
  • Ability to work independently and as a team member
  • Ability to handle multiple tasks and exercise independent judgment
  • Strong attention to detail and focus on quality of work
  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
  • Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)

 REQUIREMENTS:

  • Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
  • Skill sets and proven performance equivalent to the above

 

 

#LI-MP1

The Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

 

RESPONSIBILITIES:

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
  • Maintain and quality audit to assure the most recent revisions of documents are on project portals
  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
  • Maintain version and quality control of project documentation and submit to trial master file
  • Assist with the tracking and maintenance of project related information, including site medical question and answer log
  • Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
  • Maintain current participating site and personnel information
  • Arrange and track the distribution of project specific training to the project team

 SKILLS AND ABILITIES:

  • Excellent written and verbal English as well as fluency of the language of the country of location
  • Strong interpersonal skills
  • Ability to work independently and as a team member
  • Ability to handle multiple tasks and exercise independent judgment
  • Strong attention to detail and focus on quality of work
  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
  • Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)

 REQUIREMENTS:

  • Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
  • Skill sets and proven performance equivalent to the above

 

 

#LI-MP1

The Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

 

RESPONSIBILITIES:

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
  • Maintain and quality audit to assure the most recent revisions of documents are on project portals
  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
  • Maintain version and quality control of project documentation and submit to trial master file
  • Assist with the tracking and maintenance of project related information, including site medical question and answer log
  • Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
  • Maintain current participating site and personnel information
  • Arrange and track the distribution of project specific training to the project team

 SKILLS AND ABILITIES:

  • Excellent written and verbal English as well as fluency of the language of the country of location
  • Strong interpersonal skills
  • Ability to work independently and as a team member
  • Ability to handle multiple tasks and exercise independent judgment
  • Strong attention to detail and focus on quality of work
  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
  • Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)

 REQUIREMENTS:

  • Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
  • Skill sets and proven performance equivalent to the above

 

 

#LI-MP1

City:

State: Vojvodina

Employment Type: Regular

Community / Marketing Title: Clinical Trials Associate (Serbia)

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: Belgrade, RS

CountryEEOText_Description:

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