PSI CRO

Data Manager for Clinical Trials

Brazil full-time Mid Salary not listed
full-time Mid level Technology & IT Curated
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About the role

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
Based in Brazil
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

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

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.
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.
Originally posted on Himalayas

Interview prep

Walk in with sharper answers.

Use this as a quick practice sheet before you speak with the employer.

Mid
Technology & IT MySQL SQL Data Manager Clinical Mid level

Likely questions

  1. Tell us about work you have done that is close to the Data Manager for Clinical Trials role.
  2. How would you approach your first 30 days at PSI CRO?
  3. Which of MySQL, SQL and Data have you used recently, and what did it help you achieve?
  4. Describe a time you solved a problem without waiting to be told exactly what to do.
  5. How do you handle busy days, changing priorities, or pressure at work?

Prepare before the call

  • A recent example that proves your experience with MySQL, SQL and Data.
  • One short story with a problem, your action, and the result.
  • Two examples that show the strengths listed on your CV.
  • A clear reason why this role and company interest you.
  • Your availability, preferred work style, and salary expectations.

Ask them

  • What would success look like in the first 90 days?
  • What are the main problems this hire should help solve?
  • How does the team give feedback and measure good work?
  • What does a normal working week look like for this role?
Practice line

I am interested in the Data Manager for Clinical Trials role because I can bring practical experience in MySQL, SQL and Data, learn the team quickly, and contribute to the outcomes PSI CRO needs from this hire.

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