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Immediate Openings for Clinical Process Associate @ Thane (mumbai) (Walk In)


Hi Greetings from Technosoft Corporation !! About Technosoft: Technosoft is an integrated Information Technology (IT) and Business Process Management (BPM) solutions provider. Our collaborative culture and work environment helps attract and retain exceptional talent which is a key ingredient to address our clients needs, and help drive our sustained growth. Our biggest differentiators include: A Focused Service Portfolio Customer-Centric Approach Outcome-Based Model Exceptional Talent Culture of Curiosity and Confidence Technosoft has approximately 3,600+ employees worldwide. Our global footprint spans across North America, India, UK, Australia and New Zealand, and the Middle East. Our vision is to be partner and employer of choice in our chosen segment. For more information, visit us at Specialties: IT Consulting, BPM services, Healthcare IT, Data Sciences, Mobility, Global In-house Centers, Professional Staffing. Immediate requirement for"Clinical Process Associate" in Thane (Mumbai) Location. Contact : Vani B (9182991774) Forward Your Updated CV to : Job Description : Experience 6 Months - 5 Years (Clinical Process Associate) Notice Period: Immediate Should be flexible with Thane location Skills required - CRC knowledge, Patient Data knowledge, ICH - GCP, ICF, Adverse Events/ SAEs, site monitoring, remote site monitoring knowledge. (eTMF - experience - not mandatory but preferred).PURPOSE Provide project related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics meets quality and time line metrics.RESPONSIBILITIES Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines Establish and maintain effective project/ site communications Create and maintain relevant project documents Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information Participate in document management (creation, review, maintenance, storage, as applicable) REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines Strong written and verbal communication skills including good command of English language Results and detail-oriented approach to work delivery and output Good problem solving skills Good planning, time management and prioritization skills Attention to detail and accuracy in work Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint Ability to establish and maintain effective working relationships with coworkers, managers and clients. Proven ability to work on multiple projects balancing competing priorities Ability to coach/ mentor junior colleagues Schedule interview : If above Requirements matches to your profile can send your updated CV to : and reach at 9182991774 (drop me a text message)* Note : Ignore, if JD not matches to your profile & Do Refer to your Friends & ColleaguesRegards Vani B Salary: INR Attractive...!! Industry: Pharma / Biotech / Clinical Research Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology Role Category: Medical Professional Role: Clinical Researcher Employment Type: Permanent Job, Full Time Keyskills: clinical process traineeclinical researchclinical trialspharmaceuticalich - gcp guidelinesClinical Process AssociateSenior Clinical Process AssociateClinical Research Associate

Openings : 1




Fresher To 5 years

Valid Till

Jun 27, 2018 To Jul 27, 2018




Not Disclosed by Recruiter


Clinical Researcher




10:00am - 05:00pm


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