Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
We seek a Project Support Coordinator t to contribute to our mission to enable customers to make the world healthier cleaner and safer. Youll provide support to Clinical Data Management (CDM) project teams by performing various administrative activities.
Runs test data for user acceptance testing during startup and submits for filing
Generates user acceptance testing data files post testing for filing in the eTMF
Completes test logs for filing
Prepares study-specific metrics reports distributes reports to teams and files reports in study SharePoint folders
Cleans patient tracker at a set frequency
Performs file reviews of the eTMF using the CDM Mapping Guidance and the Database Modification Matrix
Requests access to the electronic data capture (EDC) environment for CDM users
Creates and maintains study information for CDM teams for all new and released study team members
Submits requests to grant or revoke access to the database and reviews team members system accesses
Assists with validation of a clients coding dictionary subscriptions to MedDRA and WHO Drug
Ensures a client has current and valid dictionary subscriptions and files subscription confirmations in a studys SharePoint folder and eTMF
Performs a quality control review of the content of documents uploads and classifies final study documents in PPDs eTMF to final approved status
Assists with customizing posting and filing study-specific training materials including submitting requests for training codes
Generates training completion reports and assists with training compliance verification
Files approved and final versions of CDM documents and any other documents upon Clinical Data Team Lead request to the CDM Project Documentation SharePoint folder
Performs tasks associated with generation of data review utility (DRU) listings for all functions at a frequency specified in a studys Data Validation Manual
Generates test case report forms or patient data reports from a user acceptance testing environment
Organizes writes distributes and files meeting minutes
Circulates posts and files meeting information (materials and attendee list)
Generates applicable reports from various systems (e.g. Clarity) and sends to CDM resource managers
Performs Medidata site creation for CDM stand-alone studies
Participates in patient data report (PDR) quality control review and performs PDR filing and PDR generation processes in Medidata EOS Site Cloud
Qualifications:
Education and Experience:
Bachelors degree is preferred (Preferred Fields of Study: Pharmacy Nursing Medical Technology Biology or related field)
Clinical-related experience is an advantage
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 0 to 4 years).
Knowledge Skills and Abilities:
Ability to work in a team or independently as required
Good organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively
Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Good time management skills including flexibility to reprioritize workload to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations (if required) ICH Good Clinical Practices and organization/Client SOPs and WPDs/work instructions for all non-clinical/clinical aspects of project implementation execution and closeout
Good English language and grammar skills and proficient local language skills
Effective oral and written communication skills
Good computer skills proficient in MS Office (Word Excel and PowerPoint) and ability to obtain knowledge and learn the required clinical trial systems
Ability to successfully complete CRG training program
Self-motivated positive attitude and good interpersonal skills
Required Experience:
IC
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make...
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
We seek a Project Support Coordinator t to contribute to our mission to enable customers to make the world healthier cleaner and safer. Youll provide support to Clinical Data Management (CDM) project teams by performing various administrative activities.
Runs test data for user acceptance testing during startup and submits for filing
Generates user acceptance testing data files post testing for filing in the eTMF
Completes test logs for filing
Prepares study-specific metrics reports distributes reports to teams and files reports in study SharePoint folders
Cleans patient tracker at a set frequency
Performs file reviews of the eTMF using the CDM Mapping Guidance and the Database Modification Matrix
Requests access to the electronic data capture (EDC) environment for CDM users
Creates and maintains study information for CDM teams for all new and released study team members
Submits requests to grant or revoke access to the database and reviews team members system accesses
Assists with validation of a clients coding dictionary subscriptions to MedDRA and WHO Drug
Ensures a client has current and valid dictionary subscriptions and files subscription confirmations in a studys SharePoint folder and eTMF
Performs a quality control review of the content of documents uploads and classifies final study documents in PPDs eTMF to final approved status
Assists with customizing posting and filing study-specific training materials including submitting requests for training codes
Generates training completion reports and assists with training compliance verification
Files approved and final versions of CDM documents and any other documents upon Clinical Data Team Lead request to the CDM Project Documentation SharePoint folder
Performs tasks associated with generation of data review utility (DRU) listings for all functions at a frequency specified in a studys Data Validation Manual
Generates test case report forms or patient data reports from a user acceptance testing environment
Organizes writes distributes and files meeting minutes
Circulates posts and files meeting information (materials and attendee list)
Generates applicable reports from various systems (e.g. Clarity) and sends to CDM resource managers
Performs Medidata site creation for CDM stand-alone studies
Participates in patient data report (PDR) quality control review and performs PDR filing and PDR generation processes in Medidata EOS Site Cloud
Qualifications:
Education and Experience:
Bachelors degree is preferred (Preferred Fields of Study: Pharmacy Nursing Medical Technology Biology or related field)
Clinical-related experience is an advantage
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 0 to 4 years).
Knowledge Skills and Abilities:
Ability to work in a team or independently as required
Good organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively
Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Good time management skills including flexibility to reprioritize workload to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations (if required) ICH Good Clinical Practices and organization/Client SOPs and WPDs/work instructions for all non-clinical/clinical aspects of project implementation execution and closeout
Good English language and grammar skills and proficient local language skills
Effective oral and written communication skills
Good computer skills proficient in MS Office (Word Excel and PowerPoint) and ability to obtain knowledge and learn the required clinical trial systems
Ability to successfully complete CRG training program
Self-motivated positive attitude and good interpersonal skills
Required Experience:
IC
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