Clinical Data Manager II

3 weeks ago

New Delhi, India Innovaderm Research Full time

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


Our company:

OUR COMPANY 

 

The work environment

At Innovaderm, 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. 

 

You will be eligible for the following perks: 

  • Flexible schedule
  • Vacation
  • Home-based position
  • Ongoing learning and development

 

About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe.

 

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. 


Innovaderm only accepts applicants who can legally work in India. 



Education

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


Experience

  • 10 years of clinical data management experience in the pharmaceutical industry or in a CRO environment
  • 5 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

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