Senior Techinical Designer
- Employer
- Labcorp
- Location
- Philadelphia County, Pennsylvania, US
- Salary
- Competitive
- Closing date
- Jan 15, 2022
View more
- Sector
- Consultancy/Private Sector
- Field
- Conservation science
- Discipline
- Other
- Salary Type
- Salary
- Employment Type
- Full time
You need to sign in or create an account to save a job.
Job Overview:
Senior Technical Designer(Senior Rave Programmer)-Remote
Education/Qualifications:
Senior Technical Designer(Senior Rave Programmer)-Remote
- Responsible for designing the eCRF in leading EDC systems including Rave, Veeva, Inform or
other EDC systems. - Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency.
- Follow attention to detail approach and participate in sponsor meetings and audits/inspections.
- Assign tasks and responsibilities to team members, in a manner that: optimizes team capability; delivers timely and accurate results; and supports the needs of the business.
- Assist Managers in data collection for productivity, Quality, timelines and resource planning.
- Responsible for performing quality control procedures for specification development.
- Conducts team meetings and provide guidance to Programmers and Data managers.
- Responsible for maintaining study specifications for assigned projects.
- Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills.
- Advance competency through participation in internal and external professional seminars and symposiums.
- Responsible for conducting Quality Control of study design for assigned projects.
- Participate in the validation of EDC studies when requested.
- Responsible for the creation and maintenance of library objects within the Global Libraries.
- Responsible for ensuring compliance of standard objects usage throughout the business.
- Responsible for the management of standard objects within the Global Libraries.
- Perform all activities related to specification development for study build and design of databases according to Standard procedures.
- Responsible for the review and approval of derivations and edit checks requested by the project teams.
- Mentor the study team in CRF Design and specification development for leading EDC databases.
- Oversees the project work of junior staff.
- Mentor and aide in staff development, and achievement of competency standards.
- Assist with the development of training programs to ensure staff, project and technical, achievement of position competencies.
- Present training programs to the technical staff regarding study build, standards maintenance, and/or change control.
- Participate in the development of global, harmonized SOPs and specific quality work instruction for technical service group activities.
- Notify project leadership of requests for out-of-scope work and advise management of changes in scope of projects to enable the timely development of change orders.
- Complete work according to Covance SOPs, Work Instructions and project specific guidelines in accordance with Good Clinical Practice.
Education/Qualifications:
- University / college degree (life sciences, health sciences, information technology or related subjects preferred).
- Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor's degree.
- Fluent in English, both written and verbal
- Minimum 6 years of relevant work experience to include data management and/or database programming and spec Design activities including 4 years in Medidata RAVE, Oracle
Inform, Veeva Vault or equivalent EDC experience. - Demonstrate excellent problem-solving skills, a proactive approach and the ability to make sound decisions.
- Demonstrated skill in leading teams, by example and mentoring staff.
- Excellent oral and written communication and presentation skills.
- Knowledge of clinical trial process and data management, CRF/eCRF Design, CDISC.
- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
- Demonstrated ability to work in a team environment.
- Demonstrated ability to handle multiple competing priorities.
- Proven interpersonal skills.
You need to sign in or create an account to save a job.
Get job alerts
Create a job alert and receive personalized job recommendations straight to your inbox.
Create alert