5 hours ago

- - - - - Senior Clinical Data Manager-Spain

Full time

- Senior
- Remote
- Remote, Spain

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Description

As a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by

- - - - - - is collected, managed, and reported clearly, accurately and securely.

This Role Will Be Perfect For You If:

- You want to work on studies end-to-end (involved from protocol review to database lock)
- You have the experience and confidence to lead multiple concurrent studies successfully as a Data Manager
- You enjoy working directly with clients and forming recommendations as needed

Responsibilities

Data Management lead

- Monitor study status (ie. enrollment, CRFs monitored/approved, etc.) on an ongoing basis
- Present deliverables to clients, gather feedback and propose solutions.
- Provide regular data status reports to the project team
- Oversee work of the Clinical Data Coordinator as required (quality, timeliness)
- Oversee vendors to ensure that timelines and deliverables meet sponsor and protocol requirements
- Is responsible for ongoing maintenance of the clinical database, including data review/cleaning during study conduct and during preparation for database lock/close.
- Conduct reconciliation between external data and data in the EDC system to ensure consistency, including reconciliation with sponsor safety databases for adverse events/SAE (Serious adverse events) data

Study setup – Technical
- Develop the data management plan (DMP)
- Build a study-specific clinical database using the EDC system:
- Design the electronic case report form (eCRF)
- Build the clinical database in the chosen EDC independently or with the support of an EDC programmer (determined based on the complexity of the system and study.
- Coordinate the validation and testing (UAT) of the clinical database
- Support the study team with the development of external systems capturing clinical data (ePRO or IWRS), ensuring that any data transfer requirements between these systems and the EDC are documented and tested appropriately.

User training and support
- Develop eCRF completion guidelines and other training material
- Conducts training for site users/monitors on the clinical database
- Activate/de-activate new users in the clinical database in response to requests from the project manager and maintain records of such request
- Respond to users requiring assistance with the EDC system

Database close/lock
- Generate data listings and reports needed for data review in preparation for database close/lock
- Ensure that data management documentation is complete and up to date in the trial master file (TMF)
- Archive the clinical database and related documents

Requirements

Education

- B.Sc. or M.Sc, or in a related field of study

Experience

- 7 years of clinical data management experience in the pharmaceutical industry or in a CRO environment
- 3 years of experience as a lead data manager
- Extensive experience working with EDC systems (experience with Medrio and Medidata Rave preferred)

Knowledge And Skills

- Highly organized and detail-oriented
- Project planning and time management skills
- Strong verbal and written communication skills in English
- Understanding of the drug development process and of applicable regulations, including Good Clinical Practices (GCP), ICH Guidelines
- Good understanding of CDISC SDTM/CDASH standards
- Knowledge of MedDRA and WHODrug dictionaries, an asset

Our Company The work environment At

- - - - - - , you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

In this position, you will be eligible for the following perks:

- Flexible work schedule
- Permanent full-time position
- Ongoing learning and development

Work location





Note that this opening is for a home-based position in India. Attendance at some meetings outside of regular business hours (primarily in the evening) is required.

About

- - - - - - A Global Clinical Leader In Dermatology! Formerly known as Innovaderm,

- - - - - - is a world-renowned expert and clinical research leader in dermatology.

We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.

- - - - - - is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively.

With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies,

- - - - - - is the ideal CRO partner for clinical needs at general scale.
- - - - - - is committed to providing equitable treatment and equal opportunity to all individuals. As such,

- - - - - - will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
- - - - - - only accepts applicants who can legally work in Spain.

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Not enough data to estimate a salary range for this role in this region yet.

This Role Will Be Perfect For You If:

- You want to work on studies end-to-end (involved from protocol review to database lock)
- You have the experience and confidence to lead multiple concurrent studies successfully as a Data Manager
- You enjoy working directly with clients and forming recommendations as needed

Responsibilities

Data Management lead

- Monitor study status (ie. enrollment, CRFs monitored/approved, etc.) on an ongoing basis
- Present deliverables to clients, gather feedback and propose solutions.
- Provide regular data status reports to the project team
- Oversee work of the Clinical Data Coordinator as required (quality, timeliness)
- Oversee vendors to ensure that timelines and deliverables meet sponsor and protocol requirements
- Is responsible for ongoing maintenance of the clinical database, including data review/cleaning during study conduct and during preparation for database lock/close.
- Conduct reconciliation between external data and data in the EDC system to ensure consistency, including reconciliation with sponsor safety databases for adverse events/SAE (Serious adverse events) data

Study setup – Technical




- Develop the data management plan (DMP)
- Build a study-specific clinical database using the EDC system:
- Design the electronic case report form (eCRF)
- Build the clinical database in the chosen EDC independently or with the support of an EDC programmer (determined based on the complexity of the system and study.
- Coordinate the validation and testing (UAT) of the clinical database
- Support the study team with the development of external systems capturing clinical data (ePRO or IWRS), ensuring that any data transfer requirements between these systems and the EDC are documented and tested appropriately.

User training and support
- Develop eCRF completion guidelines and other training material
- Conducts training for site users/monitors on the clinical database
- Activate/de-activate new users in the clinical database in response to requests from the project manager and maintain records of such request
- Respond to users requiring assistance with the EDC system

Database close/lock
- Generate data listings and reports needed for data review in preparation for database close/lock
- Ensure that data management documentation is complete and up to date in the trial master file (TMF)
- Archive the clinical database and related documents

Requirements

Education

- B.Sc. or M.Sc, or in a related field of study

Experience

- 7 years of clinical data management experience in the pharmaceutical industry or in a CRO environment
- 3 years of experience as a lead data manager
- Extensive experience working with EDC systems (experience with Medrio and Medidata Rave preferred)

Knowledge And Skills

- Highly organized and detail-oriented
- Project planning and time management skills
- Strong verbal and written communication skills in English
- Understanding of the drug development process and of applicable regulations, including Good Clinical Practices (GCP), ICH Guidelines
- Good understanding of CDISC SDTM/CDASH standards
- Knowledge of MedDRA and WHODrug dictionaries, an asset

Our Company The work environment At

- - - - - - , you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

In this position, you will be eligible for the following perks:

- Adaptable work schedule
- Permanent full-time position
- Ongoing learning and development

Work location

Note that this opening is for a home-based position in India. Attendance at some meetings outside of regular business hours (primarily in the evening) is required.

About

- - - - - - A Global Clinical Leader In Dermatology! Formerly known as Innovaderm,

- - - - - - is a world-renowned expert and clinical research leader in dermatology.

We have more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint.

- - - - - - is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach – which includes everything from protocol design and patient recruitment to trial monitoring and biometrics – provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively.

With capabilities in North America, Europe, Asia Pacific and Latin America; vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute our own studies,

- - - - - - is the ideal CRO partner for clinical needs at global scale.
- - - - - - is committed to providing equitable treatment and equal opportunity to all individuals. As such,

- - - - - - will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.
- - - - - - only accepts applicants who can legally work in Spain.

📌 Senior Clinical Data Manager-Spain (España)
🏢 Talanto
📍 España