Group Leader QC - Bioanalytical - Vimta Labs, Cherlapally Minimum:1.&nbsp;&nbsp;Doctorate/master’s degree in pharmacy/Analytical Chemistry/organic chemistry.2.&nbsp;&nbsp;Minimum 8-12+ years of experience in QC - Bioanalytical division.3.&nbsp;&nbsp;Should have knowledge on M

Scientist / Sr Scientist (Environment Department) - Vimta Labs, Ltd. Note: It’s a field job and should be willing to travel across India basis of project requirements.A minimum of 15 days they need to go to site.&nbsp;Qualification: M.Sc. / Engineering<u

Group Leader (Environment Department) - Vimta Labs&nbsp;Ltd Note: It’s a field job and should be willing to travel across India basis of project requirements.A minimum of 15 days they need to go to site. Qualification: M.Sc. /EngineeringExper

Travel Desk Executive (Male) - Vimta Labs Ltd, Hyderabad.Job Location: Shameerpet, Hyderabad.Experience: 3-5 years (Relevant work experience)CTC: As per market standards. Job Description:Typical duties and responsibilities of a travel executive include: independent h

Medical Writer - Vimta Labs Ltd, Cherlapally. Experience: 2- 6 years CTC: As per market standards. <ul><li>Experience in protocol design for Clinical trials, PK/PD study design for biosimilars, ICF preparation, CRF/eCRF review.</li><li>Well versed with study report writing and eCTD requirement for

QA Executive - Bioanalytical - Vimta Labs Ltd Exp: 1-3 years CTC: As per market standards. Location: Cherlapally, Hyderabad. Primary Responsibilities:&nbsp;<ol><li>Conduct In-process and study audits of Bioanalytical

Greetings from Vimta Labs Ltd! We have openings for Freshers (Males only) in Clinical Research at Vimta Labs, Cherlapally. Details of the job:Qualification: B.PharmExperience: FresherJob Location : Vimta Labs, CherlapallyCTC: 2.24 LPA (take home will be Rs. 13,200)Service Agreement: 3 yearsGender: Only Male as this includes Night Shifts as well. Interested candidates can share their resumes to keerthana.rojanala@vimta.com Contact:Keerthana9160712930

Sr Clinical Research Associate - Vimta Labs Ltd Qualification – M Pharm/ MSC/ Pharm D/ B Pharm Experience – 4-8 years&nbsp;&nbsp;<ul><li>Act as site monitor for a clinical trial (patients trial) projects of various therapeutic areas</li><li>Performing Quality Check of Regulatory Documents &amp; Trial Master Files </li><li>Contribute to creating Local Working Procedures/SOP and associated system documents.</li><li>Extensive knowledge in ICH GCP guideline and New Drugs Clinical Trial Rules 2019</li><li>Responsible for the preparation of CTA, MOU or any other relevant contracts with the vendors and customers as per the need of the study</li><li>Performing trial feasibilities and site identification and Site Selection Visits </li><li>Willing to travel both locally and to the outstation at least 10 to 15 days a month.</li><li>Preparation of organization/department for the purpose of Audit (Internal Audit, regulatory or Sponsor or any other form of Audit)</li><li>Responsible for performing Study initiation and monitoring visits and close out visit according to study monitoring plan.</li></ul>&nbsp;Interested candidates can share their resumes to keerthana.rojanala@vimta.com

&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Medical Investigator (Male) - Vimta Labs Ltd, Cherlapally Qualification: MBBSCTC: As per market standardsGender: Only Male&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Primary Responsibilities:&nbsp;1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ensures that Good Clinical Practices (GCP) are followed.&nbsp;2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Conduct planned studies as per protocol requirements, quality system procedures and SOPs.3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Review of pre study health records.4.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Obtain written informed consent before each Volunteer participation in the trial.5.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ascertaining that clinical data is complete, accurate and is recorded as per protocol and SOP requirements.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;6.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Assessment and documentation of UDS reports &amp; additional test reports.7.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Documentation of eligibility status.8.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Verification of daily Temperature log , Urotherm reading , Emergency medication kit&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;documentation and expired medication discarding.9.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Briefing research staff on conducting the trail and Group briefing of ICF to volunteers10.&nbsp;AE, SAE management, reporting and documentation.11.&nbsp;Monitoring the trial throughout its duration.12.&nbsp;Verifying the data entered on to the CRFs is consistent with source data.13.&nbsp;ICU maintenance including management of emergency conditions.14.&nbsp;Monitoring of Vitals documentation, ECG, Phlebotomy and X-ray procedures.15.&nbsp;Verification of X ray films and X ray report destruction.16.&nbsp;Post study reports assessments and documentation.17.&nbsp;Completion status of CRFs and &nbsp;documentation.&nbsp;Secondary Responsibilities:1.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Review of ICFs, CRFs.2.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Screening and Evaluation of Volunteers for study participation.3.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Monitoring of drug administration to volunteers. Interested candidates can share their resumes to keerthana.rojanala@vimta.com.

Vimta Labs Ltd

Group Leader QC - Bioanalytical - Vimta Labs

Scientist (Environment Department) - Vimta Labs

Group Leader (Environment Department) - Vimta Labs

Travel Desk Executive (Male) - Vimta Labs Ltd

Medical Writer - Vimta Labs Ltd

QA Executive - Bioanalytical - Vimta Labs Ltd

Trainee CRA (B. Pharm Freshers) - Vimta Labs

Sr Clinical Research Associate - Vimta Labs Ltd

Medical Investigator (Male) - Vimta Labs Ltd, Hyd