SIRO Clinpharm Pvt. Ltd Released Job Openings On 29/08/2022.Siro Clinpharm is a drug development solutions provider to the global healthcare industry. Our subject expertise gives us an edge in clinical trial management, clinical data management, medical writing, biostatistics & statistical programming & pharmacovigilance. In 1996 Dr.Gautam Daftary founded SIRO in Mumbai, India. In 2001 company started providing its services in Data Management.
Vacancy Details:
SIRO Clinpharm Pvt. Ltd Recruiting Any Graduates with 05-09+ years of experience for Clinical research Scientist Position.Complete Details for the Clinical research Scientist as follows.
Important Details :
- Location :Kumbhi
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application: 29/08/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job : Tata Consultancy Services(TCS) Hiring In Pharmacovigilance,Clinical ResearchÂ
Job Description/Skills Required
Key Responsibility 1) Productivity and Efficiency a. Project Management Related Activities • Responsible for time, cost and quality for assigned projects, business continuity, manage risks/issues/escalations and provide mitigations for assigned projects, organizing/conducting regular team meetings • Prepare Data Management Plan (DMP), project tools, trackers, templates, issue log for assigned projects b. Clinical Database Development Related Activities • Perform database design, program edit checks, external data load set up activities and ensure successful loading of external data • Create data listings/reports for assigned projects c. Data Review Related Activities • Design/Create/provide inputs to CRF, Subject Diary and CRF Completion Guidelines (CCG), Data Validation Plan (DVP) and Self-Evident Correction (SEC) Plan • Perform User Acceptance Testing (UAT) of clinical database, query management activities, reconciliation of external data from vendors (Lab, ECG etc.) and Serious Adverse Event (SAE) Reconciliation for assigned projects 2) Compliance to timelines, quality, processes & policies • Perform quality control activities as assigned and ensure assigned activities are conducted in compliance with regulatory requirements and SOPs • Ensure completeness and correctness of all training records • Work towards implementation of CDISC standards 3) Talent Management • Coaching and mentoring of the team and guide in scheduling work assignments • Ensure succession planning and optimal utilization of reportees • Perform ongoing assessment for direct reports and recommend/facilitate/impart necessary training to the team in identified gap areas and participate in knowledge sharing sessions 4) Support new and existing business • Author/Reviewer for SOPs, audit readiness and participation as required • Escalate issues in timely manner to Line Manager/Project Manager/Senior Management as required • Ensure timely submission of timesheets/functional tracking sheets • Provide suggestions for process improvements that result in time and cost saving and enhanced quality • Adhere to SLAs and defined metrics as applicable • Support in new business proposal and department strategies • Develop and strengthen relationship with client to facilitate positive feedback and overall increase in Clinical Data Management business • Evaluate and suggest feasibility of different EDC platform implementation
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