| Data Acquisition Analyst (Remote) at Remote, Remote, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=1934351&uid= From: bhuwan tiwari, Sonitalentcorp [email protected] Reply to: [email protected] Job Title Data Acquisition Analyst Job Location -Fully Remote Only EST or CST Zone candidates Duration - 6 Months+ Visa -Any Visa except H1B,cpt Mode Of Interview - Phone/Skype Note - Need LinkedIn ALL CANDIDATES MUST BE SENT WITH VALID LINKEDIN PROFILES. THEY WILL BE SCREENED BY ME EXSISTENSIVELY Job Description MUST HAVES: - Working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles. - Experience with all phases of drug development. - Solid Experience in handling Clinical data acquisition and management from external/3rd Party vendors. - May lead study level negotiation and agreement for data transfer or integration on behalf of company. - Should be able to function collaboratively (with some guidance) with all levels of employees , moderate supervision required. - Knowledge on FTP tools like GlobalScape, Clinical platforms like Veeva CDMS, Elluminate and Veeva TMF will be a plus. Job Description: 3rd Party Data Acquisition Lead (FSP) Role Profile - Serve as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level and manage study start up, conduct and close out activities. - Create external data transfer agreements, ensuring external clinical trial data are in alignment with company Standards and specifications to support data integration, analysis, and reporting. - Help and advice in setting up infrastructure for external data, to flow into company Clinical data pipelines. - Responsible for validation of all 3rd Party Data generated in clinical trial into company Clinical Data pipelines. - Develop strong and productive working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards and other Study Execution Team members. - Participate in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group in a formal inspection or audit. - Representing company in interactions with key external partners as part of company CT3 3rd Party Data Acquisition team. - Responsible for timely submission and on-going maintenance of study related 3rd Party Data Acquisition documentation in TMF. - Follow procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes. - Liaise with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.) performing services on behalf of company. - Escalate issues to CT3 leadership appropriately. Technical/Functional Expertise - Working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles. - Experience with all phases of drug development. - Solid Experience in handling Clinical data acquisition and management from external/3rd Party vendors. - May lead study level negotiation and agreement for data transfer or integration on behalf of company. - Should be able to function collaboratively (with some guidance) with all levels of employees , moderate supervision required. - Knowledge on FTP tools like GlobalScape, Clinical platforms like Veeva CDMS, Elluminate and Veeva TMF will be a plus. Thanks, Bhuwan Tiwari Sr.Technical Recruiter SoniTalent Corporation I 5404 Merribrook Lan--e, Prospect, KY, USA [email protected] Keywords: Kentucky Data Acquisition Analyst (Remote) [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=1934351&uid= |
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| 01:00 AM 15-Nov-24 |