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 re…
Skills: Clinical Data Management, eCRF Design, EDC Databases, Data Validation, Medical Coding
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 re…
Skills: Clinical Data Management, eCRF Design, EDC Databases, Data Validation, Medical Coding
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Research Associate (Level I) for FSP– Make an Impact at the Forefront of Innovation We have successfully suppo…
Skills: Clinical Monitoring, ICH-GCP, Risk-Based Monitoring, Root Cause Analysis, Site Management
Overview At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our cur…
Title: Director Medical Affairs Company: Ipsen Mexico S de RL de CV About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare D…
Skills: Medical Affairs Strategy, Clinical Study Design, Stakeholder Engagement, People Leadership, Real-World Evidence
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate (Level II) for FSP– Make an Impact at the Forefront of Innovation We have successfully supported t…
Skills: Clinical Monitoring, ICH-GCP, Risk-Based Monitoring, Root Cause Analysis, Site Management
1. Use clinical insight to locate customer training and application service requirements. Develop and deliver product application training and support to customers with the target of increasing customer usage rate and sa…
More human. More Minsait. Si te apasionan el colaborar en proyectos que tengan un impacto real en clientes top y de diferentes sectores y quieres afrontar un nuevo desafío ¡Te invitamos a convertirte en Minsaiter! Únete …
Skills: Advanced Mathematics, Statistical Analysis, Data Modeling, Python, R
Aprende Institute
Docente Entrenamiento Canino
Ciudad de México, Mexico · Remote Solely
Mid level
¡Estamos buscando un Docente Virtual de Entrenamiento Canino! ¿Te apasiona la enseñanza y tienes experiencia en el entrenamiento y cuidado de perros? ¡Esta oportunidad es para ti! Somos una plataforma de educación, enfoc…
Client Services Associate II - Hybrid - Mexico ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven …
Skills: Business Analysis, Operational Support, Linguistic Validation, Pharma Industry Knowledge, Quality Assurance
Ayúdanos a adelantarnos a las enfermedades junto con nuestra Área de Marketing. Formación requerida: Actualmente cursando carreras de Marketing, Administración de Empresas, Comunicación o afines. Mínimo 1 año para termin…
Skills: Marketing Campaign Execution, Project Coordination, Digital Analytics, Social Media Monitoring, Microsoft PowerPoint
La Posición Supervisar las actividades del laboratorio de control de calidad y asignar los recursos necesarios para garantizar que las actividades de análisis de productos, materiales e insumos se realicen en tiempo y fo…
Locations: Mexico City **This role will require full-time on-site presence (5 days / week) at our office in Mexico City)** **This role is NOT eligible for relocation assistance** About Zifo: Zifo is a leading global scie…
Skills: Business Analysis, Scientific Informatics, Requirement Elicitation, Gap Analysis, Project Management
Overview About the Role & Team IDC is seeking a Data Analyst to join the enterprise infrastructure group. In this role, you will have the opportunity to work on several of IDC's enterprise programs, including servers, st…
Skills: Market Research, Data Analysis, Predictive Modeling, Statistical Analysis, Microsoft Excel
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as an Associate Project Manager - Site Payments - Make an Impact at the Forefront of Innovation The Associate Project Manager - Sit…
Sr CTM and CTM - Mexico - Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, …
Skills: Clinical Trial Management, Site Management, ICH-GCP Compliance, Stakeholder Management, Team Leadership
Job Overview: Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as requir…
Skills: Site Activation, Regulatory Compliance, ICH/GCP Guidelines, Site Management, Contract Negotiation
Home -Based - CDMX ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, col…
Skills: Pharmacovigilance, Drug Safety, Adverse Event Processing, Regulatory Reporting, Data Collection
Home -Based - CDMX ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, col…
Skills: Pharmacovigilance, Drug Safety, Adverse Event Processing, Regulatory Reporting, Data Collection
CDMX ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, ag…
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
Full-time
bachelor degree
Posted 43d ago
~40 hrs/week
Responsibilities
The Clinical Data Manager is responsible for designing eCRFs and data validation plans while managing database set-up and maintenance. They coordinate data entry, perform QC checks, and communicate with clients and vendors to ensure high-quality clinical trial data.
Requirements
Candidates must hold a university degree in Life Sciences or Pharmacy and have demonstrated experience managing clinical or medical data. Proficiency in English and experience with systems like Medidata Rave or Oracle InForm are required.
Full 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
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.
Related keywords
Clinical Research OrganizationCROClinical TrialseCRFEDCMedidata RaveOracle InFormSAE ReconciliationDatabase LockLife SciencesPharmacyData Validation PlanMedical DataPharmaceutical Industry
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 ‘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
Offices: Baarerstrasse 113a, Zug, 6300, CH
Number One Patient Enrollment CROClinical ResearchClinical TrialsOncologyHematologyMultiple SclerosisInfectious DiseasesPatient EnrollmentPhase 2 Phase 3
How many Science & Research jobs are open in Ciudad de México, Mexico right now?
There are currently 339 open science & research positions in Ciudad de México, Mexico listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Ciudad de México, Mexico?
Companies currently hiring include ICON plc, Thermo Fisher Scientific, ALS, IQVIA, Boehringer Ingelheim, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Ciudad de México, Mexico?
Yes — 192 of the 339 open science & research positions offer remote or hybrid work (90 remote, 102 hybrid).
How do I apply for Science & Research jobs in Ciudad de México, Mexico?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.