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Clinical research coordinator jobs

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clinical research coordinator

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1

Bangalore

naukri.com -  2 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Greetings from Quintiles.We have an Opportunity for clinical research coordinator / clinical project coordinator Position.Exp: 1+yrsJob Location :Bangaloreplease find below the JD .If interested, please share updated CV with the following details.Currentc CTC:Expected CTC:...  >>

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Jobs - QuintilesJobs: Bangalore

2

Gurgaon

naukri.com -  4 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Recruitment,coordination & follow up of trial subjects, covering informed consent, adhering to safety and compliance issues;sample collection & shipment;Administer study drug;Coordination & management of Clinical Trial; >>

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Jobs - TECH OBSERVERJobs: Gurgaon

3

Belgaum

wideoffers.com -  15 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Coordinating the Clinical trials and assisting PrincipalInvestigator in successful conduct of trial in accordance to ICH-GCP guidelines, Schedule Y& Regulatory requirement,Ensure protocol adherence and complianceIndustry: Pharma/Hospitality >>

4

Pune

itsmyascent.com -  17 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

BHMS/BAMS/MBBS with 2-3 years experience in clinical research industry. Attractive salary commensurate with qualifications and experience. Job Application Details : Interested Candidates Visit our Website : & email CVs to kemvadu@kemhrcvadu.org & director@kemhrcpune.org. >>

5

Bangalore

careerage.com -  7 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Croissance Clinical Research Pvt Ltd Openings in Clinical Site Manager/Clinical Research Associate Croissance Clinical Research is a Biopharmaceutical Service provider and full service CRO, providing services to pharmaceutical, biotechnology and medical devices companies. Clinical...  >>

6

Mumbai

timesjobs.com -  11 days ago  -  [ Job details ]   -   [ Save job ]

Rs 1 Lakhs - 4 Lakhs

Working independently and proactively to coordinate all necessary activities required for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. You will be involved in the submission of protocol, consent documents for...  >>

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Jobs - ICONJobs: Mumbai

7

Secunderabad

timesjobs.com -  8 days ago  -  [ Job details ]   -   [ Save job ]

Rs 2 Lakhs - 13 Lakhs

 ...institution, and the sponsor.QualificationsLife Science Post Graduate/B.PharmaKnowledge of Indian and International Clinical trial regulations.Interest in research methodology.Detail oriented.Good organizational skills.Ability to work independently.Innovative and creative....  >>

8

Mumbai

timesjobs.com -  19 days ago  -  [ Job details ]   -   [ Save job ]

Rs 5 Lakhs - 10 Lakhs

This is an opportunity to work for ICON Clinical Research. With a track record for successful analysis and extensive scientific publication,...  ...Overview of the roleWorking independently and proactively to coordinate all necessary activities required for setting up and...  >>

9

Kolkata

naukri.com -  17 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

 ...with your site team for timely completion of the EDC and will coordinate with delegated site staff to ensure that all the relevant information...  .../Sponsor in a timely manner.Manage the inventory of all non-clinical study supplies received &/or returned at site level.Assist in...  >>

10

Hyderabad

careerage.com -  17 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Croissance Clinical Research Pvt Ltd Openings in Clinical Research Associate Croissance Clinical Research is a Biopharmaceutical Service provider and full service CRO, providing services to pharmaceutical, biotechnology and medical devices companies. Clinical Research Associate...  >>

11

Puducherry

careerbuilder.co.in [+1] careerbuilder.co.in - xpatjobs.com -  7 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Coordinating the Clinical trials and assisting Principal Investigator in successful conduct of trial in accordance to ICH-GCP guidelines, Schedule Y& Regulatory requirement, Ensure protocol adherence and compliance Industry: Pharma/Hospitality >>

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Jobs: Puducherry

12

Mumbai

naukri.com -  5 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

 ...train others in ICH-GXPs applicable for Clinical Operations Expert knowledge of and compliance...  ...to in-house KLINERA CPM.oHandling and coordinating all information pertaining to safety...  ...management. Ability to monitor clinical research sites independently Ability to...  >>

13

Visakhapatnam

naukri.com -  10 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Individual Case Safety Report Processing,End to End CDM activitiesRelevant experience in Clinical Data Management (Mandatory Rave/OC)Perform data management activities on the assigned project in a timely and efficient manner >>

14

Bhubaneswar

naukri.com -  10 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Individual Case Safety Report Processing,End to End CDM activitiesRelevant experience in Clinical Data Management (Mandatory Rave/OC)Perform data management activities on the assigned project in a timely and efficient manner >>

15

Delhi

naukri.com -  11 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

 ...activities related to the processing of clinical trial databases. Commonly performs the following...  ...CRF with SAS annotations and coordinates review and approval by internal study team...  ...appropriate action for resolution based on research of the database and CRFs./liliResolves discrepancies...  >>

16

Mumbai

naukri.com -  1 day ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

BMale candidates will be Preffered/B1. Overseeing all implementation all project specific clinical data as a QC.2. Coordinate with protocol preparation.3. Preparation of clinical study reports (CSR), Project summary.4. ICF Reviewing and obtaining of ICF.5. Reviewing of Trial...  >>

17

Bangalore

timesjobs.com -  8 days ago  -  [ Job details ]   -   [ Save job ]

Rs 1 Lakhs - 2 Lakhs

Who would ensure smooth conduct of all clinical trials sponsored by NNIPL in accordance with good clinical research practice guidelines by NN A/S and local regulatory requirements...  ...Clinical Research Associate is to coordinate with regulatory team for HA dossier preparation...  >>

18

successfactors.com

Bangalore

successfactors.com -  7 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

 ...advanced diagnostics to life-saving treatment. Posted Position Title Clinical Applications Specialist Career Level Experienced Function...  ...marketing & customers to define user needs & is engineering lead for research collaboration projects. Activities include requirements...  >>

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Jobs: Bangalore

19

Surat

careerbuilder.co.in -  9 days ago  -  [ Job details ]   -   [ Save job ]

(negotiable)

Coordinating the Clinical trials and assisting Principal Investigator in successful conduct of trial in accordance to ICH-GCP guidelines, Schedule Y& Regulatory requirement, Ensure protocol adherence and compliance Industry: Pharma/Hospitality >>

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Jobs: Surat

20

Nagpur

xpatjobs.com [+1] xpatjobs.com - www.shine.com -  10 days ago  -  [ Job details ]   -   [ Save job ]

Rs 3 Lakhs

Coordinating the Clinical trials and assisting Principal Investigator in successful conduct of trial in accordance to ICH-GCP guidelines, Schedule Y& Regulatory requirement, Ensure protocol adherence and compliance Industry: Pharma/HospitalityIch - Gcp Guidelines or Schedule...  >>

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Jobs: Nagpur

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