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Explore 47 Remote Ich Guidelines Jobs

The Medical Writer will provide clinical regulatory document support and ensure high-quality submissions in the bio-pharmaceutical industry.

CA, USA
Full-time
Writing
Precision Medicine Group logo

Senior Quality Auditor - Remote

Precision Medicine Group

6 days ago

The Senior Quality Auditor ensures compliance with regulations and provides oversight for quality and compliance activities in clinical studies.

USA
Full-time
QA
$80,000 - $120,000 USD/year
AbbVie logo

Bilingual Clinical Research Associate II - Remote

AbbVie

6 days ago

Join AbbVie as a Bilingual Clinical Research Associate II, where you will monitor clinical studies and ensure compliance with regulatory standards.

Canada
Full-time
All others

I.C

Senior Director, Medical Writing Portfolio Management - Remote

IMVT Corporation

1 week ago

The Senior Director, Medical Writing Portfolio Management, will oversee the production of high-quality regulatory documents for clinical submissions.

Worldwide
Full-time
All others
$260,000 - $280,000/year
AbbVie logo

Bilingual Clinical Research Associate II - Remote

AbbVie

1 week ago

Join AbbVie as a Bilingual Clinical Research Associate II, responsible for overseeing clinical studies and ensuring compliance with regulatory standards.

Worldwide
Full-time
All others
AbbVie logo

Bilingual Clinical Research Associate II - Remote

AbbVie

1 week ago

Join AbbVie as a Bilingual Clinical Research Associate II to monitor and ensure compliance at clinical study sites.

QC, Canada
Full-time
All others
AbbVie logo

Clinical Research Associate I - Remote

AbbVie

1 week ago

Join AbbVie as a Clinical Research Associate I to support and manage clinical trials ensuring compliance with regulatory standards.

Canada
Full-time
All others
Biogen logo

Senior Clinical Trial Specialist - Remote

Biogen

1 week ago

Biogen is seeking a Senior Clinical Trial Specialist to assist in executing clinical trials with minimal guidance while ensuring compliance with regulatory standards.

USA
Full-time
All others
$93,000 - $121,000/year

The Senior Medical Writer will write and edit clinical documents while ensuring compliance with regulatory standards.

Worldwide
Full-time
Writing

R.J.K

Director of Regulatory Labeling - Remote

Regeneron Japan KK

1 week ago

The Director of Regulatory Labeling oversees the development and management of regulatory labeling processes for pharmaceutical products.

USA
Full-time
All others
$202,000.00 - $336,600.00/year

B.U

Clinical Research Associate - Remote

BeiGene UK

3 weeks ago

The Clinical Research Associate is responsible for monitoring clinical trials and ensuring compliance with regulatory standards in the oncology field.

Worldwide
Full-time
All others
Tempus logo

Associate Clinical Trial Lead - Remote

Tempus

5 weeks ago

Join as an Associate Clinical Trial Lead, supporting clinical operations and site management for oncology trials.

USA
Full-time
All others
$110,000 - $140,000 USD/year
Clinigen logo

Senior Pharmacovigilance Project Manager - Remote

Clinigen

6 weeks ago

Clinigen is seeking a Senior PV Project Manager to lead client programs and manage pharmacovigilance activities.

USA
Full-time
Project Management
DELFI Diagnostics logo

Principal Clinical Scientist - Remote

DELFI Diagnostics

6 weeks ago

Join DELFI Diagnostics as a Principal Clinical Scientist to lead clinical studies and research collaborations aimed at improving cancer detection.

Worldwide
Full-time
All others
AbbVie logo

Clinical Research Associate I - Remote

AbbVie

6 weeks ago

The Clinical Research Associate I role involves managing clinical trials and ensuring compliance while working remotely.

USA
Full-time
All others