Site Management Associate I

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

College/University Degree, preferably in Life Sciences., Proficiency in standard MS Office applications and English., Good organizational, planning, and problem-solving skills., Detail-oriented with the ability to multi-task in a fast-paced environment..

Key responsibilities:

  • Support clinical research projects by streamlining communication and managing documents.
  • Exchange data and information between investigative sites, vendors, and project teams.
  • Ensure proper administration of site payments and regulatory submissions.
  • Maintain the Trial Master File and prepare for audits and inspections.

PSI CRO AG  logo
PSI CRO AG Pharmaceuticals Large http://www.psi-cro.com
1001 - 5000 Employees
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Job description

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 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

This role is hybrid - Based in Bucharest

Job Description

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

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 (preferably Life Sciences)
  • Proficiency in standard MS Office applications
  • Proficiency in English
  • 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

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.

Required profile

Experience

Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Office
  • Communication
  • Multitasking
  • Teamwork
  • Customer Service
  • Detail Oriented
  • Physical Flexibility
  • Social Skills
  • Problem Solving

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