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Clinical Research Job Vacancies in Jalgaon

Chemist (2-5 Years)

TPS Consultancy

  • 2 - 5 yrs
  • 0.9 Lac/Yr
  • Chalisgaon Jalgaon
LAB Equipment Clinical Research
Designation :- ChemistQualification:- BSc/MSc/B.Tech In Food Or Equivalent Experience :- 2 Years To 5 Years In Process Industry Salary:- As Per InterviewGender:- MaleJob Description:- i) All instrument calibration / solution preparation / standardization.ii) To execute finished product testing as per standard protocol.iii) To be carried out analysis of Coal in Coal plant in absence of their permanent chemist.Also carried out on line finished product analysis & monitoring in process labv) To be carried out maize Rack analysis as per plan.vi) To follow Lab Safety PPEs during analysis in lab.vii) To preserve control sample in lab and also send marketing sample or to customer asper Requirements.To maintain Housekeeping in Central Lab.To follow & maintain Central Lab as per GLP standard.Also have knowledge of handling & Testing:-1)Hplc2)GC3)UV spectrophotometer4)Karl Fisher5)Bomb calorimeter6)Sap7)Raw material chemical & packing testing8) Brookfield viscosity9)Water testing10)Chemical preparation and std.12) Final product all testingJob Location:- Chalisgaon, Maharashtra Industry:- Manufacturing Company
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Clinical Research Medical Coder Clinical Coordinator
Key Responsibilities:1. Trial Architecture:> Contribute to the development of dynamic trial plans and protocols in tandem with the clinical operations team.> Collaborate on the strategic selection and qualification of investigative sites.2. Site Symphony:> Conduct harmonious site initiation, monitoring, and close-out visits to ensure seamless protocol execution and pristine data collection.> Cultivate collaborative relationships with investigative site teams, providing support and guidance.3. Regulatory Mastery:> Ensure meticulous adherence to regulatory standards, guidelines, and the principles of Good Clinical Practice (GCP).> Spearhead the preparation and submission of regulatory documents to ethics committees and regulatory authorities.4. Data Choreography:> Direct the orchestration of data collection, ensuring the accuracy and completeness of clinical trial data.> Collaborate with data management teams to resolve data discrepancies and maintain a symphony of data quality.5. Risk Ballet:> Proactively identify potential risks to trial success and choreograph mitigation strategies in collaboration with project teams.6. Communication Sonata:> Cultivate clear and resonant communication channels with internal and external stakeholders.> Compose eloquent and timely study progress reports, fostering transparency and accountability.Qualifications:Bachelor's or advanced degree in a relevant field (Life Sciences, Nursing, etc.).Demonstrated experience as a Clinical Research Associate, preferably in the pharmaceutical or biotechnology domain.Profound knowledge of clinical trial processes, regulatory requirements, and GCP.Exceptional interpersonal and communication finesse
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