Clinical Study Reports Jobs

Expert Medical Regulatory Writer

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

regulatory writing Periodic Benefit-Risk Evaluation Report Health Authorities Queries CTD submission documents Briefing packages immunogenicity reports risk management plans publication submission trial transparency documents clinical evaluation report Clinical Study Reports therapeutic area/domain knowledge exposure medical section global registration of drugs Product Alerts project management

13 days ago

Expert Medical Regulatory Writer

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

Health Authorities Queries Product Alerts publication submission project management Clinical Study Reports regulatory writing medical section Periodic Benefit-Risk Evaluation Report global registration of drugs trial transparency documents risk management plans therapeutic area/domain knowledge exposure Briefing packages immunogenicity reports CTD submission documents clinical evaluation report

10 days ago

Scientific Writer II

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

2-4 years

Medical Organizational regulatory documentation Clinical Study Reports Scientific Facilitation Interpersonal Skills Document Management System global pharmaceutical drug development communication

13 days ago

Clinical Research Physician

Permanent Job

Chennai ,

India

0-2 years

Patient Safety Clinical Study Reports study sites Interpersonal Skills GCP standards team-oriented environment medical expertise fast-paced investigators clinical research clinical trial processes ethical research practices Regulatory Submissions clinical trial protocols communication

20 days ago

Pharmacovigilance Services Associate

Permanent Job

Bengaluru / Bangalore ,

India

1-3 years

CIOMS patient services solutions Clinical Study Reports Problem-solving skills Pharmacovigilance Operations stakeholders Regulatory Pharmacovigilance Regulatory Results orientation Written And Verbal Communication Clinical Qc RD Safety Writing Life Sciences data listings Affiliate Mailbox Narrative Writing Regulatory Submissions Clinical Submission Narrative Writing safety reports Project Lead

24 days ago

Global Clinical Publishing Associate

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

Fresher

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

a month ago

Associate Manager - Scientific Writing

Permanent Job

Bengaluru / Bangalore ,

India

8-12 years

DataVision Clinical Study Reports publication planning publication writing Microsoft Tools medical slide decks Scientific Writing Infographics scientific communications platform pharma regulations PubsHub PM Solution therapeutic areas manuscripts publication guidelines medical communications PLS

a month ago

2500_ Medical Writer

Permanent Job

Bengaluru / Bangalore ,

India

0-2 years

management monitoring briefing documents risk facilitation Clinical Study Reports clinical documents process improvement NDA/MAA CTD submission documents Training toolkit generation documentation/archiving Assessment Audit regulatory authority questions protocols investigator brochures Inspection Capacity Building change management Performance

a month ago

Medical Writer (Freshers)

Permanent Job

Aurangabad ,

India

1-3 years

scientific documents Clinical Study Reports Medical Terminology protocol summaries Regulatory Submissions Microsoft Office Suite scientific literature

a month ago

Senior Statistical Programmer

Permanent Job

Bengaluru / Bangalore ,

India

5-7 years

technical and regulatory requirements R Clinical Study Reports Pooling Safety data clinical drug development commercialization Regulatory Submissions scientific data SAS

a month ago

Senior Medical Writer

Permanent Job

Bengaluru / Bangalore ,

India

5-7 years

Organizational Skills Time Management Clinical Study Reports Protocols Editing Budget Management Mentorship Proofreading Clinical Research Scientific Communication Project Management Medical Writing literature reviews Regulatory Submission Documents

5 months ago

Functional Quality Specialist I

Permanent Job

Pune ,

India

0-2 years

drug safety data management process improvement initiatives training material voice calls quality errors bridging reports periodic adverse drug experience reports regulatory inspections Clinical Trials protocols medical device audit readiness Data Analysis medical information Clinical Study Reports quality management plan Process Review process improvement training schedule global regulatory submissions technology solutions product quality complaints patient access Quality Management periodic safety update reports therapeutic areas Annual Reports clinical development regulatory agencies investigator brochures safety reports

4 months ago

Senior specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

Clinical Study Reports Data Analysis Regulatory Compliance Lifesciences Documentation Management Operational Excellence

4 months ago

Senior specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

Clinical Study Reports Data Analysis Regulatory Compliance Lifesciences Documentation Management Operational Excellence

4 months ago

Senior specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

4 months ago

Specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

4-6 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

4 months ago

Manager

Permanent Job

Remote ,

India

4-6 years

ICH-E6 Clinical Trial Documents Clinical Study Reports data analyses Statistics E3 guideline template for Protocol regulatory documents Informed Consent Form protocol

4 months ago

Medical Writing

Permanent Job

Bengaluru / Bangalore ,

India

5-7 years

Financials project management Clinical Study Reports Time Management scientific communication scientific data business development Regulatory Requirements editing Messaging clinical research Budgets literature reviews Proofreading protocols Organizational Skills

3 months ago

Senior specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

4 months ago

Specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

4-6 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

4 months ago

Senior specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

8-10 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

5 months ago

Specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

4-6 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

4 months ago

Specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

4-6 years

Lifesciences Operational Excellence Clinical Study Reports Documentation Management Data Analysis Regulatory Compliance

5 months ago

Specialist - RegOps IM

Permanent Job

Hyderabad / Secunderabad, Telangana ,

India

4-6 years

Clinical Study Reports Data Analysis Regulatory Compliance Lifesciences Documentation Management Operational Excellence

4 months ago

Senior Medical Writer

Permanent Job

Bengaluru / Bangalore ,

India

5-7 years

Organizational Skills Time Management Clinical Study Reports Protocols Editing Team Environment Proofreading Clinical Research Scientific Communication Messaging literature reviews Regulatory Submission Documents

5 months ago

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Clinical Study Reports Jobs

Expert Medical Regulatory Writer

Expert Medical Regulatory Writer

Scientific Writer II

Clinical Research Physician

Pharmacovigilance Services Associate

Global Clinical Publishing Associate

Associate Manager - Scientific Writing

2500_ Medical Writer

Medical Writer (Freshers)

Senior Statistical Programmer

Senior Medical Writer

Functional Quality Specialist I

Senior specialist - RegOps IM

Senior specialist - RegOps IM

Senior specialist - RegOps IM

Specialist - RegOps IM

Manager

Medical Writing

Senior specialist - RegOps IM

Specialist - RegOps IM

Senior specialist - RegOps IM

Specialist - RegOps IM

Specialist - RegOps IM

Specialist - RegOps IM

Senior Medical Writer