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Open nowPosted 14 hours agoWe saw it 44 min after it went up

Site Management Associate (Clinical Trials)

PSI CRO175 open roles

Where
Ra'anana, Center District, Israel
Work mode
On site
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Your applicationOpen nowSite Management Associate (Clinical Trials)PSI CRO · Ra'anana, Center District, Israel

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

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The clock on this job

Early applications get read.

12.7% of postings close within 7 days. Measured by our own scanner across the market. PSI CRO postings stay open a median of 13 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.5%3 days
  3. 12.7%7 days
  4. 20.4%14 days
  5. 35.6%30 days
  6. 58.7%60 days
This job: posted 14 hours ago

PSI CRO median: 13 days open

The posting

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. You will focus on facilitating research projects of novel medicinal products, while taking a step further in your professional career.

Office-based role in Ra'anana, Israel

The scope of responsibilities will include:

Performs site management activities, documents and trackers management, and communication with the sites and study vendors.

Site Management and Communication

  • 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 regulatory and ethics committee submissions and notifications
  • Ensures proper administration of sites and vendors payments, as applicable
  • Coordinates preparation for and follow-up on site, TMF and systems´ audits and inspections
  • Reviews and coordinates site-specific EDC completion and provides the site Monitor with regular updates on the completion status
  • 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 and performs TMF oversight at country/site level
  • Prepares, distributes, and updates Investigator Site Files and ISF checklists
  • Revises and checks translation status

Safety Management

  • Ensures proper safety information flow with investigative sites

CTMS Management

  • Updates CTMS with project information
  • Supports Monitors in completion of all subject and site events information in CTMS, and meeting deadlines for site visits and visit reports

Qualifications

  • College/University Degree (Life Sciences)
  • Prior administrative experience in Clinical Research / CRO environment, preferably in an international setting
  • Full working proficiency in Heberw and good English skills
  • Proficiency in standard MS Office applications (Word, Excel and PowerPoint)
  • Good organizational and planning skills, problem-solving abilities, 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

*Please send your CV in English

Additional Information

As a privately owned mid-size CRO, we are constantly growing, offering plenty of opportunities for personal and professional growth.

Our extensive onboarding and mentorship program will prepare you to fulfil your tasks with the highest standards, offering you:

  • Excellent and flexible working conditions
  • A unique combination of team collaboration and independent work
  • Competitive salary and benefits package
  • Opportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success.

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