| Hot C2C opening for Business Systems Analyst (Clinical Trials-Rave of Medidata) Remote role at Remote, Remote, USA |
| Email: [email protected] |
| From: Gobi, PiplNow [email protected] Reply to: [email protected] Hello, Greetings from PiplNow LLC I have an urgent C2C opening for Business Systems Analyst (Clinical Trials-Rave of Medidata) Remote role Experience 8+ years Our client is looking to fill this role immediately. Please share your updated resume, Filled skill matrix and consultant details asap. Skills Matrix: Skills Years of Experience Overall Experience Business Systems Analyst Clinical Trail Management System (CTMS) Medi-data Rave applications EDC (Electronic Data Capture) Project Management Regulatory submissions, reporting, and audits eTMF (electronic Trial Master file) Environmental Health & Safety rules Consultant Details: Criteria Consultant's Data Full Name Primary Phone Primary Email Education (highest degree with major, year of graduation and name of institute) Certification if any LinkedIn Profile US work authorization and expiration Expected payrate on C2C Current Company Name Current location (City/State) Willing to relocate (yes/No) Availability to join new project/ Notice period Have you ever worked or interviewed for this client in the past If yes, as a consultant or as an employee Last 5 digits of Social Security Number Birth month and day (NOT YEAR) Role: Business Systems Analyst (Clinical Trials-Rave of Medidata) Job Location: Remote Job ID: ZR_344_JOB Experience: 8-15 Years Key Responsibilities: Over 9+ Years of experience working as Business Systems Analyst with strong Understanding of global Life sciences and the industry's challenges Experience working on Medidata Clinical Trail Management System (CTMS) Hands-on experience working on Medidata Rave applications and Safety systems background. Extensive experience in EDC (Electronic Data Capture) Ability to carry out research and in-depth analysis (qualitative/quantitative) to arrive at strategic insights Work with clinical staff and providers and help in crafting the templates, content, and workflow as each specialty dictates. Work with the technical, development, integration, design, implementation, and support teams for any query regarding the product and its enhancements, crafting solutions to address end-user requirements. collaborate with cross-functional business and technology teams to design and deliver complex applications and solutions to clients across healthcare and medical devices entities. Own the entire product development lifecycle from mapping requirements, testing, implementation, and validation. Evaluate user requests, perform business, and process analysis, gather business requirements, develop functional specifications, develop test scripts, and perform unit and Evaluate business processes and develop process improvement/optimization recommendations where needed Identify business and analytics needs in close partnership with stakeholders, capture data requirements and translate them into language which can be understood by technology and solutions teams Create visualizations and dashboards to help the company interpret and make decisions with the data Requirements Education and Experience: Bachelor's Degree in scientific or related field with 8 years previous clinical trial management or Master's Degree or equivalent in a related discipline Additional Skills: Proven successful project management skills Proven expertise in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred Excellent problem-solving, organizational, analytical and critical thinking skills including high discretion/judgment in decision making Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives Expert understanding of regulatory submissions, reporting, and audits Knowledge of financial mechanism that relates to clinical trials Demonstrated ability to manage assigned team and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations Ability to develop and integrate metrics into the projects and operations that clearly demonstrate the value of clinical trials to the business Strict attention to detail Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization Ability to work and excel within a fast paced, dynamic, and constantly changing work environment Frequently interacts with customers, and/or functional peer group managers, normally involving matters between cross-functional teams and the company; often leads a cooperative effort among members of a project team Participate and present at meetings with internal and external representatives Resolve operational and scheduling issues Dedicated to quality client service and pro-active and responsive to client needs. Develop peer, cross functional and cross business relationships to maximize best practice sharing and team effectiveness. Develop relationships and leverage them to influence change Support and solicit input from team members at all levels within the organization Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control Thanks & Regards Gobinath. B Vice President - Client Success | PiplNow, LLC Keywords: |
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| Fri Dec 09 00:33:00 UTC 2022 |