Open vacancy for entry level clinical data management, responsibilities can be characterized, but not limited to, the collection, tracking, management and maintenance of study related documentation and interaction with sites and study staff as directed. Activities will normally be routine in character.
Qualifications and Education Requirements
Bachelor’s degree and/or other medical qualification or relevant Data entry experience preferred.
Knowledge / Skills
Intermediate computer skills preferred.
High interpersonal skills.
Meticulous, time management, team work, stress management, and punctuality.
Interview is scheduled on 12 and 13 October at 12:00 pm
Company Information:
DataClin Organization
Job Specification Text:
Key Accountabilities Track and receipt paper CRF Perform DE as per study specific convention Transcription, entry and verification of clinical trials source data into case report forms of various formats. Interface with other department personnel on all transcription and/or data entry issues. Assistance in performing quality control. Provide technical support to assigned projects for example download, copy and keeping records of all electronic data. Assist with record keeping, quality control and filing of study documents according to DataClin SOPs. Create Central Files for new studies and maintain Central Files for ongoing studies according to DataClin SOP’s or contractual obligation to sponsor Track, scan, code, file and retrieve documents as required for project team members. Complete routine administrative tasks in a timely manner Photocopy, print and distribute documents, as needed Enter clinical trials data into the appropriate database Ensure up to date study documents in tracking systems Develop study related plans in coordination with DM. Maintain quality control procedures to ensure accurate maintenance of files. Develop CRF annotation according to CDASH standards. Develop/review project plans, including data entry conventions, data management plan, data validation plan, QC plan. Develop database entry screens, perform test, EC and validation. Perform coding as required. Maintain a working knowledge and ensure compliance with applicable ICH-GCP Guidelines, local regulatory requirements and DataClin SOP and study specific procedure
Applying Email:
bd@dataclin.com
