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Clinical Programmer Analyst - Senior

Mercerville, NJ 08619

Posted: 04/03/2024 Employment Type: Contract Job Category: Data Sciences Job Number: 603839 Is job remote?: Yes Country: United States

Job Description


Target Pay Rate: 40-56/hr **salary will be commensurate with experience 

Qualifications:
  • Minimum 10 years of relevant work experience to include data management and/or database programming and spec Design activities including 10 years in Medidata RAVE
  • Strong Programming skill set
  • Knowledge of Python, building dashboards
  • Knowledge of API programming
  • 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

Responsibilities:
  • Senior Rave Programmer Responsible for designing the eCRF in leading EDC systems in Rave
  • Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles.
  • Provide technical support and troubleshooting for Rave study development as well as site management and user access within supported RAVE modules
  • Serve as system administrator to grant user access using iMedidata Cloud Administration for RAVE EDC, Coder, Lab Admin, RTSM and MMI (Imaging) provide Oversight, guidance, and design of study build activities on Rave URL.
  • Create Advanced Analytics dashboards
  • Insights into creating actionable dashboards and deep understanding and knowledge of good interpretation of clinical data
  • Responsible for the preparation and /or review draft and final eCRF, edit check specifications for assigned projects to ensure quality and consistency
  • Responsible for conducting Quality Control of study design for assigned projects and participate in the validation of EDC studies
  • 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
  • Participate in the development of global, harmonized SOPs and specific quality work instruction for technical service group activities
  • Complete work according to SOPs, Work Instructions and project specific guidelines in accordance with Good Clinical Practice


**CO/NY candidates may not be considered 

The staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.

Planet Pharma and The Planet Group of Companies are equal opportunity employers. It is our practice not to discriminate against any employee or applicant based on any criteria, condition or basis protected by laws or regulations in the locations where we do business. All qualified applicants are encouraged to apply. We celebrate diversity and are committed to providing an environment of mutual respect. We believe that diversity, equity and inclusion enable us to better meet our mission and values while serving our clients across the globe. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter, or contact us, so that we can discuss the appropriate alternatives available.

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About Mercerville, NJ

Ready to take the next big step in your career? Explore job opportunities in and around Mercerville, New Jersey - where growth and opportunity await! Nestled in the heart of Mercer County, Mercerville boasts a charming blend of suburban tranquility and urban excitement. With easy access to cultural landmarks like Grounds For Sculpture and Patriots Theater at the War Memorial, as well as tantalizing cuisine like tomato pies from nearby Trenton, this region offers a unique mix of art, entertainment, and culinary delights. Consider joining the thriving job market surrounded by lush parks, such as Veterans Park, or catching a game at the Trenton Thunder stadium. Discover the irresistible charm of Mercerville and kickstart your career today!

Although this hasn't been an issue at Planet Pharma, the staffing industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly and never provide banking information during the application process. Candidate safety is a top priority at Planet Pharma.