Vacancy at Veeda Clinical Research for Research Associate, QA and more

Multiple vacancies for Research Associate(Clinical, Bio-analytical and Project managment), Quality Monitor,Project Coordinator and Clinical Research Physician  in Veeda Clinical Research organisation at Ahmedabad location.

 

Research Associate for Bioanalytical Research

No. of Vacancies: 5

Qualification:  M.Pharma./ M.Sc.

Location:  Ahmedabad

Experience: 1 to 5 years

 

Job Responsibilities:

1. Bioanalytical method development, method validation and project sample analysis
2. Sample Preparation in bioanalytical lab as per method SOPs
3. Biological Sample Movement (e.g. to manage biological plasma sample, blood sample, urine sample, serum samples etc.)
4. Operation, Maintenance and calibration of equipments (refrigerated centrifuge, pH meter, analytical balance, micropipettes, HPLC, LCMS etc.)
5. Maintaining the equipment log(s)
6. Review bioanalytical data
7. Inform group leader about the progress or completion of the assigned activity
8. Contingency arrangement
9. Maintenance of displays (labels, SOPs, Charts etc.)
10. Supervision of the general laboratory activities
11. Reply to relevant QC/QA queries in co-ordination with team members
12. Execution and maintenance of GLP, GCP, Safety and Quality systems

 

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Quality Monitor : Clinical Research

No. of Vacancies: 3

Qualification:  B.Sc. / B.Pharma.

Location:  Ahmedabad

Experience: 0 to 1 years

Job Responsibilities:

1.) Review the Protocol, Informed Consent Documents (ICD) (English and/or vernacular language), Case Report Form (CRF) and/or associated working documents related to study and suggest any change to concern CRD personnel.
2.) Ensure that all the study personnel are been trained on the study protocol and duties are appropriately delegated, before initiation of any study related activities.
3.) Review the screening records of all the subjects to ensure the eligibility for study participation.
4.) Monitor all the following study specific activities (but not limited to) to ensure compliance to the protocol and the governing SOPs: (a) ICD presentation and obtaining to the volunteer (at screening or in period:01 only) to ensure that sufficient time is given to the volunteers to decide their participation in the study before signing the ICD. (b) Screening of volunteers. (c) Protocol Compliance assessment etc. (d).All study related activities during execution.
5.) Monitoring of Clinical Facility: Monitor the clinical facilities (but not limited to) for availability of adequate SOPs, SOP compliance, completeness and correctness of log-books, calibration, maintenance and labeling of equipments.
6.) Audit/Visit: Ensure the respective clinic/facility is ready for audit/visit
7.) Review all the study related documents (CRF and source documents) to ensure the completeness, correctness and compliance to the protocol, SOP & applicable regulatory guidelines and documentation of deviations, if any

 

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Biopharmaceutics & Project Management

 

No. of Vacancies: 2

Qualification:  M.Pharma. (Pharmacology).

Location:  Ahmedabad

Experience: 1 to 2 years

 

Job Responsibilities:

1. Preparation of Study documents:
• Coordinate with the Project Manager (PM), Principal Investigator (PI) and/or Clinical Investigator (CI), Bioanalytical team, and Statistician, for protocol preparation
• Prepare Informed Consent Documents (ICD) in English and coordinate for translation into Local language(s) and it’s back translation into English, if applicable.
• Preparation of the CRFs and other working documents, if applicable.
• Prepare documents for submission to the regulatory.
• Incorporate the protocol comments received from Investigator, QC, QA, BR and Sponsor before finalization of the same.
2. Feasibility of the study proposal
• Assist PM for feasibility assessment of study proposal.
• Literature survey for PK & Safety study.
3. IEC Communication:
• Coordinate with Principal Investigator (PI) and/or Clinical Investigator (CI) for application
• Prepare documents for submission to the Ethics Committee (EC).
4. Dose administration activity as required.
5. Perform any other duties as assigned by line manager.

 

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Project Coordinator: Clinical Research

No. of Vacancies: 2

Qualification:  M. Pharm.

Location:  Ahmedabad

Experience: 1 to 2 years

Job Responsibilities:

1.) Preparation of Study documents
2.) Ensure NOC, Approval letter from the IEC, Availability of IPs are available before study execution.
3.) Study Planning and Execution
4.) Coordinate with the pharmacist and PM for Procurement, Handling, Storage, Dispensing (as per the randomization list), Accountability and Retention / Disposal / Retrieval of investigational products (IP).

 

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Clinical Research Physician (CRP): Clinical Research

 

No. of Vacancies: 3

Qualification:  MBBS 

Location:  Ahmedabad

Experience: 0 to 3 years

 

Job Responsibilities:

1 Protocol, Informed Consent From (ICF), case report form (CRF) Preparation
2 Ethics submission
3 Subject Recruitment/ Screening
4 Clinical examination of the subjects and monitoring activities
5 Handling adverse events and clinical emergency
6 Ensure subjects safety
7 Documentation works
8 Report preparation:
9 Feasibility assessment

 

 

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1 responses on "Vacancy at Veeda Clinical Research for Research Associate, QA and more"

  1. Send me updates of clinical research and pharmacovigilence. Thank you

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