Cliantha Research Walk In Interviews For Analyst – Large Molecule Lab on 09th Dec, 2023 |Freshers & experience
Experience: 0 – 5 Years
6 Vacancies
Job Profile:
The Analyst responsibilities should include, but not be limited to the following functions:
Access to the study plan and appropriate Standard Operating Procedures applicable to their involvement in the study.
Under direction of the project manager, performs method development, method validation and study sample analysis experiments.
It is their responsibility to comply with the instructions given in the forms of documents.
Any deviation from the instructions should be documented by the analyst and communicated directly to the Study Director, and/or if appropriate, the Principal Investigator(s).
All analysts are responsible for recording raw data promptly and accurately and in compliance with these Principles of Good Laboratory Practice, and are responsible for the quality of their data.
Analyst should exercise health precautions to minimize risk to them and to ensure the integrity of the study.
In case of multi site study, analysts are required to follow approved SOPs from another test site; any additional training required should be documented.
There may be some sites where temporarily employed personnel carry out aspects of study conduct. Where these persons have generated or entered raw data, or have performed activities relevant to the conduct of the study, records of their qualifications, training and experience should be maintained.
Analyst should ensure the pre-clinical/non-clinical studies are following the approved protocols, study plans, amendments to protocol/study plan, applicable regulatory guidelines and in-house standard operating procedures.
Analyst must have a copy of the study plan and if there are any amendments that should be communicated in timely manner and effectively with the study and QA personnel as required during the conduct of the study.
Analyst should ensure that unforeseen circumstances that may affect the quality and/or integrity of the study are noted when they occur and that corrective and preventive actions are taken immediately and documented.
calibration and preventive maintenance of pipettes.
Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Clianthas mission is Science with Integrity. Cliantha has eighteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Cliantha Research is headquartered in India with facilities in Ahmedabad, Noida and Vadodara. Cliantha has a presence in USA (facilities in Florida and Project Management in New Jersey), Canada (facilities in Mississauga, Winnipeg and Scarborough) and Portugal (Project management).
Time and venue
09th Dec, 2.00 PM – 5.30 PM
3rd Floor, Commerce House II, Above Fab India, Opp. Pushparaj Towers, Judges Bungalow Road, Bodakdev 380054
Contact – Sanjay Chauhan (8780992926)
