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Job Details

Site ID Services Specialist 2 (f/m) - office based in Stockholm

Company: Quintiles
Location: Uppsala
Reference: 1712009
Closing Date: 30 Aug 17
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

This is a crucial role within QuintilesIMS and the opportunity to start or progress your career in clinical research. With this position, we are offering a variety of development options for e.g. an experienced Site ID Services Specialist, a CRA/SrCRA who is looking for a new challenge in an office based role. ...

Requirements:

This is a crucial role within QuintilesIMS and the opportunity to start or progress your career in clinical research. With this position, we are offering a variety of development options for e.g. an experienced Site ID Services Specialist, a CRA/SrCRA who is looking for a new challenge in an office based role.
You will manage study site identification process for an assigned region in accordance with applicable local and/or international regulations, our companies? standard operating procedures and project requirements.
As Site ID Services Specialist, you will be accountable for and involved in the selection of the sites, the feasibility activities and correspondence with the responsible investigators. As a person, you enjoy building relationships and you enjoy working cross-functionally within an international environment. You are able manage multiple projects, to prioritize tasks and to dig into details when needed.

 
 
RESPONSIBILITIES

  • Manage assigned opportunities / projects / programs for country or region and adhere to timelines and budget.
  • Generate site list of appropriate investigators in accordance with the needs of the sponsor and specifications of the protocol
  • Coordinate collection and analysis of country / regional Feasibility / Site Identification information to meet timelines of proposal process and independent feasibility assessments
  • Reconcile and interpret Feasibility / Site Identification data to provide country level assessments and recommendations for country site numbers, recruitment rates, timelines and screen failure rates
  • Distribute, track, negotiate and review the Confidential Disclosure Agreements (CDAs) for Feasibility / Site Identification with assistance from Management / Legal department as appropriate
  • Distribute, track and review Site Questionnaire Forms for Feasibility / Site Identification for completeness, site capability and suitability of investigators
  • Manage the investigator database entry and quality, ensuring complete investigator and site information is captured, and monitor for duplicate entries
  • Maintain and update company information repositories and databases
     
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
  • Sound knowledge of medical terminology, GCP, FDA regulations, and Drug Development process and procedures.
  • Strong communication, organizational and interpersonal skills.
  • Proficient in the use of Microsoft Office, Presentation skills and team training.
  • Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
  • Strong negotiation skills.
  • Strong verbal and written communication including good command of English language
  • Ability to handle multiple tasks with varying deadlines.
  • Ability to maintain confidentiality.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

 

Bachelor's degree in life sciences or related field, with 3 years? relevant experience including demonstrable experience in acting as the main local lead in studies or equivalent combination of education, training and experience.

 

 

Apply for this job: Site ID Services Specialist 2 (f/m) - office based in Stockholm

Contact Information:

Address:  .
.

England
Website:  Visit Our Web Site

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