Site Management Associate

Posted Yesterday
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Banja Luka, Republika Srpska, BIH
In-Office
Entry level
Pharmaceutical
The Role
Supports clinical research projects by coordinating communication with investigative sites and vendors, managing clinical supplies and payments, facilitating regulatory and ethics submissions, maintaining Trial Master Files and Investigator Site Files, tracking study information, supporting audits and meetings, and ensuring safety information flows appropriately. The role is office-based in Banja Luka and requires medical or pharmacy education, strong organization, multilingual communication, and Microsoft Office proficiency.
Summary Generated by Built In
Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information.

This role is office-based in Banja Luka, Bosnia and Herzegovina

Communication and Site Management

  • Exchanges data, documents and other project relevant information between investigative sites, site vendors and the project team, and with other PSI departments
  • Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies
  • Ensures proper administration of sites and vendors payments, as applicable
  • Ensures regulatory and ethics committee submissions and notifications
  • Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections
  • Supports the organization of internal team meetings including preparation of agendas and minutes, and also of Investigator’s Meetings
  • Maintains study-specific and corporate tracking systems

Document Management

  • Maintains Trial Master File (TMF)
  • Performs TMF review and oversight at country and site level
  • Prepares, distributes, and updates Investigator Site Files (ISF) and ISF checklists
  • Revises and checks translation status

Safety Management

  • Ensures proper safety information flow with investigative sites

Qualifications

  • College/University Degree in Medicine or Pharmacy
  • Prior administrative experience is a plus
  • Proficiency in standard MS Office applications
  • Full working proficiency in English, Bosnian and Serbian
  • Good organizational and planning skills, problem-solving abilities, and flexibility
  • Detail-oriented, able to multi-task and work effectively in a fast-paced environment
  • Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects

Additional Information

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.

Please submit your resume in English.

Skills Required

  • College or university degree in Medicine or Pharmacy
  • Proficiency in standard Microsoft Office applications
  • Full working proficiency in English, Bosnian, and Serbian
  • Good organizational and planning skills
  • Problem-solving abilities and flexibility
  • Detail-oriented, able to multitask, and effective in a fast-paced environment
  • Team-oriented with excellent customer service and interpersonal skills
  • Prior administrative experience
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The Company
HQ: Zug
1,939 Employees
Year Founded: 1995

What We Do

PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com

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