Data

Work From Anywhere; México; A distancia; MXN 360.000 - 540.000; Jornada completa

Descripción de la vacante

PSI is a leading Contract Research Organization with 30 years of experience in the pharmaceutical industry. Open to candidates in Mexico, we seek a Clinical Data Manager to manage clinical or medical data with accuracy and efficiency.

You will track database setup, testing, maintenance and data entry, coordinate with clients and vendors, design eCRFs and data plans, ensure data validation, and train site staff. English proficiency and experience with Medidata Rave or Oracle InForm are required.

Formación

• Degree in Life Science or Pharmacy is a plus.
• Experience managing clinical or medical data.
• Proficiency in English is required.

Responsabilidades

• Track database set-up, testing, maintenance and data entry.
• Communicate with clients, project teams and vendors on data management matters.
• Review study documents and design project guidelines.
• Design eCRF, Data Management and Data Validation Plans.
• Ensure data entry, follow-up and validation including CRF review.
• Code medical data and report metrics to database lock.
• Coordinate processing, dispatch and archiving of CRFs/queries.

Conocimientos

English proficiency

Data management

Time management

Independent work

Educación

College/University degree in Life Science or Pharmacy

Herramientas

Medidata Rave

Oracle InForm

MS Office

Descripción del empleo

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.

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.

Ready?

Open to: Mexico.

Australia, Canada, France, Germany, India, United Kingdom, United States