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| Ascentrik Research Pvt. Ltd Pune Job For B.Tech/B.E./ MSc in Bio-Chemistry/Bio-Technology/ M.Pharm |
Job Description
Qualification:
Masters in Pharmacy/Chemistry/Bio-Chemistry/Bio-Technology (B.Tech/B.E. in Bio-Chemistry/Bio-Technology
MS/M.Sc(Science) in Biotechnology, Bio-Chemistry, M.Pharma in Pharmacy
Ph.D in Biotechnology)
Candidates with masters degree is eligible
Candidates with additional Clinical research diploma or relevant courses will be preferred
Candidate should have basic computer skills, Microsoft Office & detailed Internet Knowledge
Vacancies: 15
Salary: ₹ 2,50,000 - 3,00,000 P.A
Location- Wakad, Pune, Maharashtra
Designation: Clinical Research Associate
Ascentrik Research Pvt. Ltd is a premier Research & Data Service Provider serving the Top Fortune 500 Companies & many more Multi-National Companies across different industries & sectors. We are pioneers in customized Research Services and are providing actionable insights with quality data to our clients. We are operating with a large work force from offices in Pune, Navi Mumbai and are aiming to grow even more. We are looking out for a Clinical Research professional who has a relevant experience and has excellent knowledge. Below is the detailed job description.
Job Description:
We are looking for a Clinical Research Associate with at least 0.6-1 year of relevant experience. A highly organized person, with excellent coordination, communication and team management skills and must have Clinical research experience.
Skills & Responsibilities:
Strong knowledge on various phases and types of trials
Good understanding of Efficacy, safety, biomarker expressions, interventions and familiar with medical terms related to oncology study would be advantageous
Should help in organizing and monitoring the different phases of clinical trials of different
drugs and track & coordinate changes with on-shore team
Understanding of clinical trial sources and different trial registries
Collecting and authenticating data from conference and publications
Keep a regular track on the updates in trials/reports using multiple sources
Excellent knowledge about websites like Pub Med, Clinicaltrials.gov, Abstracts, Annual reports etc. will be preferred
Quick learner and ability to grasp new technologies
Should be able to conduct 100% quality check of all the documents, rectifying the errors before submitting the work for execution
Must be able to work in deadline driven environment & be able to handle various assignments
Interested candidates can drop their updated resume and contact details on khuntia.sonali@ascentrik.com
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