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  • 5 - 8 Years
  • Posted : above 1 month

Job Description:

- Reviewer to perform authoring, standalone QC, data QC and    scientific review of publication deliverables like Manuscripts,   Abstracts, Posters, Slide Decks, Literature Review etc - Compliance to timelines, quality, processes & policies and   robust tracking of revenues, resource utilization and budget - Robust review of Publication Writing documents (Manuscripts,   Abstracts, Posters, Slide Decks, Literature Review etc) in   accordance with documented guidelines, SOPs, and timelines - Ensure that the data is objectively and accurately represented   Responsible for the final deliverable in terms of timelines and   quality - Optimal project utilization ensuring maximum productivity per   assigned work load and defined metrics - Ensure that documents are approved and issued as per   timelines and comply with established quality standards and   performance metrics - Strict adherence to applicable processes and policies,   including but not limited to applicable regulations, guidelines,   policies, SOPs, WIs, process flows, templates, style guides, etc - Ensure timely reporting of deliverables, project updates &   prompt issue escalation to the line manager/ project manager;   perform any other responsibility assigned by Line Manager - Support department promotional activities assigned by   reporting manager/ business leads - Be prepared for any audits and inspections with maintaining all   systems and processes up to date

Profile Summary:

Employment Type : Full Time
Eligibility : UG: BDS - Dentistry,
MBBS - Medicine,
BHMS - Any Specialization,
BAMS - Any Specialization,
B.Pharma - Pharmacy
Industry : Pharma, Biotech, Clinical Research
Functional Area : Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology
Role : Documentation/Medical Writing
Salary : Not Disclosed by Recruiter
Deadline : 18th Feb 2020

Key Skills:

Company Profile:

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 DrGautam Daftary founded SIRO in Mumbai, India In 2001 company started providing its services in Data Management Bio statistics and a Medical WritingThe 1st breakthrough was made in 2007 when SIRO was awarded the Frost & Sullivan Partner of Choice award for clinical trials in India SIRO won the title Clinical Research Organization of the Year by Frost and Sullivan for the 2nd time in a row for their India Healthcare award in 2012 And also received the Life Science Leader award for capabilities in Regulatory, Productivity, Reliability and Accessibility

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