reputed company / reputed company RAVE System Designer/Programmer

reputed company: reputed company (reputed company reputed company) - Fortune Pharmaceuticals MUST HAVE 8+ YEARS OF reputed company . Job Descriptio n: Position Title: reputed company / reputed company RAVE System Designer/Program merLocation: Rem oteContract Period: 12 Mon thsShift Timings: Mon - Fri, 08:00 AM - 05:00 PM Length of contract: 1 Year extended for 2nd year, post PE.Location/Site: Prefer - New Jersey or reputed company to another reputed company office, but reputed company to any location if they the experie nce.Purp

• ose:Data Science is the best-in-class team reputed company its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from reputed company data. Our operational model is exemplified through execution and innovat
• ion.This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Clinical Data reputed company Organizat

ion.Manager's Upd ate:Initially this is a remote role 1st Preference is finding candidates on Florham Park, NJ 07932 or reputed company reputed company New Je rsey If it will convert moving reputed company then they need to work hybrid in Chicago, IL, Floram Park, NJ, and Irvine , CA Manager is reputed company to consider 100% remote initially but after converting into permanent/FTE they have to be hybrid (3 days onsite & 2 days remote per week. | Usually Mon & Fri: Remote and Tue - Thu: Ons

• ite)This is a system design
• roleEDC Programmer/reputed company reputed company reputed company of reputed company are requ
• iredMust have reputed company. with reputed company
• RAVEPrior reputed company. with reputed company Vault would be reputed company to
• haveMust have reputed company. with reputed company (Electronic Data Capt
• ure)reputed company to coordinating with other team members such as Statistician, program
• mer,Must have reputed company. with CDASH and SDTM control termino
• logyProtocol trading reputed company set is requ
• iredTA: SkinCare, EyeCare, Specilaity Phase I, Immunology, Neurology and Onco
• logyMust have prior leadership level reputed company. so that they will reputed company to work with the study
• teamMust have good understanding of GCP and ICH guidel
• inesMust have good understanding of busi
• nessMust have good communication sk
• illsAble to work independe
• ntlyReal time hands-on reputed company. is requ
• iredPhD/MS with right years of hands-on reputed company. would be consider
• ablePrior any TA is
• fineMust have 7+ years of reputed company. (More reputed company. would be more bet
• ter)There is no such overqualification reputed company involved in this
• roleProtocol reading reputed company set is requ
• iredMedidata RAVE certification would be a plus but not at reputed company requ
• iredMinimum educational qualification: BS De

greeResponsibilit

• ies:reputed company participates in the development of common data standards and ensures systems designs reputed company with the standards, as reputed company as with associated protocol requirements. Ensures that the design team utilizes stand
• ardsEstablishes and maintains methodology used by reputed company to design and reputed company clinical trial systems, benchmarking against industry standards. Ensures that systems are specified to optimize functionality, end user experience, and data reputed company. Ensures that the design team meets these expectat
• ionsEnsures that TA- and program-level consistency is achieved by the design
• teamAccountable for the on-time design and delivery of new clinical systems, integration between systems, as reputed company as any required changes to clinical systems (e.g., reputed company, IRT, ePRO). Utilizes project management tools to reputed company study reputed company and plan work. Anticipates and identifies issues that could reputed company timelines or reputed company and develops reputed company and solut
• ionsInteracts with and influences CDO and cross-functional team members to reputed company program and study objectives. Ensures that assigned work product is synchronized with upstream and reputed company dependen
• ciesEnsures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, reputed company reputed company Operating Procedures (SOPs), and functional reputed company standards. Stays abreast of new and/or evolving local regulations, guidelines and policies reputed company to clinical reputed company
• mentResponsible for coaching and mentoring members of reputed company, as reputed company as contributing to their reputed company reputed company
• mentLeads CDO and cross-functional innovation and process improvement initiat

ivesQualificat

• ionsBachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Masters prefer
• red.Must have 7+ years of hands-on technical Study build in reputed company. Experience with technical study build in reputed company RAVE is required. reputed company reputed company technical study build experience is a p
• lus.In-depth knowledge of clinical trial proces
• ses.In-depth knowledge of CDASH (Required) and S
• DTM.Demonstrated performance as a key contributor to initiatives and advancement of the organizat
• ion.Demonstrated ability to influence others without reputed company authority. Demonstrated ability to successfully reputed company / mentor in a matrixed environment. Demonstrated effective communication skills and analytical ski

lls. Apply To This Job