116

Clinical Study Jobs

Senior Manager - AGM - Clinical Research

Permanent Job

Gurugram ,

Gurgaon / Gurugram ,

India

16-17 years

regulatory queries clinical overviews communication Budget Management SOP compliance project execution Coordination Vendor Negotiation vendor approval clinical project contracts study reports cro management

27 days ago

Associate Medical Writer

Permanent Job

Bengaluru / Bangalore ,

India

2-4 years

Medical Writing real-world studies study protocol pharmaceutical Knowledge Sharing abstracts literature searches congress posters audit-preparedness Presentations Regulatory Requirements Process Improvements study report clinical document version reviews healthcare industry therapy areas Collaboration communication

22 days ago

MICC Executive

Permanent Job

Ahmedabad ,

India

1-3 years

Pharmacovigilance CRO setup medical information inquiries Regulatory Requirements safety reporting clinical monitoring Audits good documentation practices Programme Management GxP Compliance Engineering Services Plant Setup GCP Auditing Study Design Csv

a month ago

Centralized Study Spec II

Permanent Job

Bengaluru / Bangalore ,

India

0-2 years

issue resolution risk identification vendor oversight management study performance dashboard compliance metrics Process Improvements Clinical Systems technology solutions study payments patient access project scheduling tools Collaboration study specific reports clinical development project management systems trial master file documentation project plans communication Data Management Monitoring Tools

a month ago

Senior Centralized Study Asso

Permanent Job

Bengaluru / Bangalore ,

India

0-2 years

ctms Project Management Systems Vendor Management oversight technology solutions TMF study payments patient access IWRS clinical development Data Review Xcellerate Risk Identification & Issue Resolution (XRIM) EDC

a month ago

Clinical Trial Manager

Permanent Job

Bengaluru / Bangalore ,

India

0-2 years

sponsor Delivery Health Insurance therapeutic area Risk Mitigation flexible benefits Clinical Trial Management Monitoring performance goals enrolment retirement planning clinical research life assurance Vendor study start-up Budget cross-functional teams Reporting metrics

a month ago

Lead Clinical Database Programmer

Permanent Job

Bengaluru / Bangalore ,

India

6-8 years

Rave Custom Functions Word Clinical Data Management Medidata Rave Study Build C# Gcp Excel Sdlc

a month ago

Medical Writing / Research Analyst

Permanent Job

India

1-3 years

Cro proprietary data study designs Molecular Biology Biotechnology Organic Chemistry regulatory documents Industry Multiple Projects collaborative self-starter Drug oncology conference meeting reviews Oncology peripheral computer equipment internet sources scientific story scientific understanding major cancer conferences Pharm. D. professional appearance authorship protocols Immunology Biology typical office equipment Motivated Data Analysis internal oncology meetings study reports peer-recognized journals publication research clinical trial research Publications deadline-driven environment pharmaceutical company Biochemistry Organized Microsoft Office Suite Secondary Research Reports

a month ago

Site Management Associate

Permanent Job

Bengaluru / Bangalore ,

India

1-3 years

eTMF clinical research study budget vendor management MS teams Office Excel

a month ago

Oncology Clinical Operations Asset Lead, Director

Permanent Job

Bengaluru / Bangalore ,

India

0-10 years

risk management Delivery clinical operations project management Relationship Building Team Management Resourcing Oncology phase 2 mitigation plans Conflict Management feasibility phase 1 clinical research Leadership Budgets Negotiation Stakeholder Management Study Management matrix management communication Data Quality

a month ago

Clinical Research Scientist II

Permanent Job

Navi Mumbai ,

Mumbai ,

India

0-2 years

Medical precautions Mbbs Clinical Investigator Regulatory Requirements protocol contradictions IB declaration Of Helsinki dosing label study schedule stations EC dosing information adverse events Sponsor warnings Icd BABE Studies ethical principles vacutainer labels Lotus SOP Clinical drug interaction CRF Gcp

a month ago

Nursing Tutor for (College of Nursing)

Permanent Job

Thane ,

India

2-4 years

online learning platforms medical-surgical nursing Pharmacology Time Management clinical practice Study Skills anatomy and physiology pediatric nursing Nursing Education NCLEX-style questions

a month ago

Senior Statistical Programmer

Permanent Job

India

5-7 years

CRF libraries Conferences regulatory documents Sops data presentation compliance with applicable regulatory agency guidelines TFLs professional association committee work cdisc standards data submission packages CDASH Data Storage automating statistical programming tasks Clinical Studies corporate policies Study Design industry forums ADAM programming conventions data dictionaries progress tracking Sas Programming Sdtm Protocol Development Sas Macros SAP Statistical Analysis Data Transformation

a month ago

Associate Medical Writer

Permanent Job

Bengaluru / Bangalore ,

India

2-4 years

Medical Writing Knowledge Sharing Collaboration pharmaceutical congress posters therapy areas healthcare industry Process Improvements abstracts real-world studies Regulatory Requirements study report audit-preparedness study protocol communication Presentations investigator"s brochures clinical document version reviews literature searches non-interventional study reports

a month ago

Sr. Clinical Research Associate

Permanent Job

Gurgaon / Gurugram ,

India

4-5 years

SIV ICH GCP Training IMP supply scheme ancillary supplies audits SAE reporting site related details IRB submissions patient facing compliance issues quality oversight visits TMF risks site invoices Lab kits Pd Inspections site management ITF investigator meetings study progress essential documents management regulatory submission e-diaries study recruitment risks Dm cross-functional units IMP supplies deliverables on-site monitoring site related payments sites closeout visits on-site visits quality data review recruitment recruitment retention strategies PI oversight Patient Safety retention materials clinical trial agreements site feasibilities site selection visits Medical team CRO monitor Market CRA clinical research Budgets geographic scope India Cluster Quality

a month ago

Officer/ Sr. Officer

Permanent Job

Mumbai ,

India

0-2 years

clinical operations raw data Sop bioequivalence department facility audit study reports Process Audit

5 months ago

Clinical Research Associate

Permanent Job

Pune ,

India

1-4 years

Clinical study supplies TMF ICH GCP Regulatory Compliance site management OSF adverse events Investigational Product Data Quality

5 months ago

Clinical Research Assoc II

Permanent Job

Bengaluru / Bangalore ,

India

3-5 years

clinical research associate training diverse recruitment job opportunity Documentation contract research organizations essential documents teva s equal employment opportunity commitment Vendors sex ethnic origin ancestry central monitoring ich-gcp accessible candidate experience Workplace study managers age legally recognized status Sops TMF study database tgec study-related documents gender identity color race disability employment accommodations teva pharmaceuticals creed veteran status applicable laws equal opportunity knowledge collection accommodation information expression bpgs national Selection Process sexual orientation study conduct inclusive pregnancy medical condition quality control procedures manager clinical research religion Csm Gcp Csom

4 months ago

Senior Clinical Programmer

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

2-4 years

clinical data management system (CDMS) applications relational database structures JReview Interpersonal Skills Clinical Programming Business Objects iMedNet knowledge FDA regulations biostatistics analysis clinical research company SOPs Installation data quality edit checks reporting application development database build specifications Validation data entry screens Medidata Rave EDC Certified Study Builder Certification C# Spotfire database administration Technical Documentation Sas Programming

3 months ago

Clinical Research Coordinator II

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

2-4 years

Study Documentation Study Progress Clinical Research Investigation Data Collection Study Protocols

4 months ago

CLINICAL PROJECT ASSOCIATE

Permanent Job

Mumbai ,

India

0-1 years

Study Progress Clinical Research Study Initiation CSR writing DCGI Gcp Data Management

5 months ago

Regulatory Affairs Manager

Permanent Job

Bengaluru / Bangalore ,

India

5-7 years

clinical trial submissions study timelines clinical trial submission dossiers regulatory dossiers feasibility research regulatory aspects Regulatory Requirements bid defense meetings Vendors Clinical Trials problem-solving skills communication regulatory authorities regulatory-related matters project teams legislative acts project planning documents Import and Export license applications clinical research regulations Ms Office Applications Collaboration safety issues client presentations

5 months ago

Clinical Research Coordinator

Permanent Job

Mumbai ,

India

0-2 years

Clinical Research regulatory guidelines Institutional Policies Clinical Research Studies Study Data Study Sponsors Study Protocols Study Team Members Study Participants Study Assessments

5 months ago

Data Analytics Manager

Permanent Job

Bengaluru / Bangalore ,

India

0-2 years

Study Report health authorities regulatory files Investigator?s Brochure competent medical officer Data Listing review scientific and medical quality project scientific community clinical safety data registration process scientific data Regional Evidence Generation Epidemiology study conduct potential safety signals Clinical Research external scientific meetings Local Medical Leads study results protocols medical and human safety clinical portion Clinical Programs ethical conduct Good Clinical Practices clinical trial Good Epidemiology Practice study reports individual studies serious adverse events clinical/epidemiology studies clinical development peer review journals Accountable GEP therapy area epidemiology study protocols clinical trial synopses medical consistency regulatory guidelines labelling medical portion Gcp

5 months ago

Veeva Vault

Permanent Job

India

0-2 years

Vault EDC Veeva Clinical Study Startup Site Connect Veeva Products Vault eTMF Vault CTMS Agile Scrum Jira

5 months ago

Home

clinical study Jobs

Top Industry

Job Category

Clinical Study Jobs

Senior Manager - AGM - Clinical Research

Associate Medical Writer

MICC Executive

Centralized Study Spec II

Senior Centralized Study Asso

Clinical Trial Manager

Lead Clinical Database Programmer

Medical Writing / Research Analyst

Site Management Associate

Oncology Clinical Operations Asset Lead, Director

Clinical Research Scientist II

Nursing Tutor for (College of Nursing)

Senior Statistical Programmer

Associate Medical Writer

Sr. Clinical Research Associate

Officer/ Sr. Officer

Clinical Research Associate

Clinical Research Assoc II

Senior Clinical Programmer

Clinical Research Coordinator II

CLINICAL PROJECT ASSOCIATE

Regulatory Affairs Manager

Clinical Research Coordinator

Data Analytics Manager

Veeva Vault