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Data Manager for Clinical Trials

Role overview

Qualifications

  • College/University degree (Life Science, Pharmacy degree is a plus)
  • Demonstrated experience of managing clinical or medical data
  • Full working proficiency in English
  • Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)

Responsibilities

  • Track database set-up, testing, maintenance and data entry
  • Communicate with clients, project teams and vendors on data management matters
  • Review study documents, design and develop project specific guidelines and instructions
  • Design eCRF, Data Management and Data Validation Plans and test EDC databases

Key facts

Other skills

  • Microsoft Office
  • Organizational Skills
  • Time Management
  • Communication
  • Multitasking

About the company

PSI CRO AG  logo

PSI CRO AG

Pharmaceuticals

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 β€˜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

Company details

Company typeLarge
IndustryPharmaceuticals
Company size1001 - 5000

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Job description

Company Description

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.

We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.

Job Description

Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.

Please submit your CV in English

Responsibilities will include:

  • Track database set-up, testing, maintenance and data entry
  • Communicate with clients, project teams and vendors on data management matters
  • Review study documents, design and develop project specific guidelines and instructions
  • Design eCRF, Data Management and Data Validation Plans and test EDC databases
  • Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation
  • Code medical data
  • Track and report metrics leading to database lock
  • Coordinate the processing, dispatch and archiving of CRFs/queries
  • Maintain Clinical Data Management working files
  • Perform database QC checks, prepare and attend audits
  • Train site staff and project teams on CRF completion and data management topics

Qualifications

  • College/University degree (Life Science, Pharmacy degree is a plus)
  • Demonstrated experience of managing clinical or medical data
  • Full working proficiency in English
  • Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm)
  • Proficiency in MS Office applications
  • Organisational and time management skills
  • Ability to work independently and multi-task

Additional Information

Base salary range: €34,000–€52,000 gross annual salary.
Actual compensation: The salary offered within the stated range will depend on objective, job-related criteria, including demonstrated competencies, qualifications, and skills relevant to the position.
Additional compensation: bonus, incentive plans, and other benefits may apply.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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