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Explore 50 Remote Regulatory Documents Jobs

ELLIGO HEALTH RESEARCH logo

Project Management Specialist, Optimized Trials - Remote

ELLIGO HEALTH RESEARCH

4 days ago

The Project Management Specialist will coordinate and support the operations of clinical trials at Elligo.

Worldwide
Full-time
Project Management

A.B

Senior TMF Specialist (Contractor) - Remote

Arcus Biosciences

2 weeks ago

The Senior TMF Specialist will manage regulatory documents for clinical trials, ensuring compliance and quality.

USA
Contract
All others
ELLIGO HEALTH RESEARCH logo

Project Management Specialist, Optimized Trials - Remote

ELLIGO HEALTH RESEARCH

10 weeks ago

The Project Management Specialist will coordinate and support clinical trial operations and regulatory compliance.

Worldwide
Full-time
Project Management
MERIT CRO logo

Project Manager I - Remote

MERIT CRO

10 weeks ago

The Project Manager I will oversee clinical trial project management, ensuring effective operations from start-up to closeout.

USA
Full-time
Project Management

Celcuity

Associate Director, Medical Writing - Remote

Celcuity

11 weeks ago

The Associate Director, Medical Writing will oversee the creation and quality control of regulatory documents in the oncology field.

Worldwide
Full-time
Writing
$200,000 - $230,000/year
BioMarin Pharmaceutical logo

Senior Medical Writer - Remote

BioMarin Pharmaceutical

12 weeks ago

The Senior Medical Writer will draft and edit clinical documents and collaborate with cross-functional teams in a biotechnology setting.

USA
Full-time
Writing
Dianthustherapeutics logo

Director, Clinical Development Scientist - Remote

Dianthustherapeutics

15 weeks ago

Lead clinical development initiatives for Myasthenia Gravis while supporting the APAC region in a remote role.

USA
Full-time
All others

C.B

Senior Manager, Medical Writing - Remote

Cogent Biosciences

15 weeks ago

Seeking an experienced medical writer to lead the development of clinical and regulatory documents in a biotechnology company.

USA
Full-time
Writing
130000 - 180000 USD/year
Ergomed logo

Senior Medical Writer with Line Management Experience - Remote

Ergomed

15 weeks ago

Join PrimeVigilance as a Senior Medical Writer to lead a team and contribute to drug safety documentation.

India
Full-time
Writing
Spyre Therapeutics logo

Senior Medical Writer - Remote

Spyre Therapeutics

16 weeks ago

The Senior Medical Writer will author and contribute to clinical and regulatory documents, ensuring compliance with ethical and regulatory standards.

Worldwide
Full-time
Writing
$130,000 - $145,000/year

D.T

Associate Director, Medical Writing - Remote

Dyne Therapeutics

20 weeks ago

The Associate Director, Medical Writing is responsible for preparing high-quality clinical and regulatory documents for Dyne Therapeutics.

Worldwide
Full-time
Writing
$194,000 - $213,000 USD
AbbVie logo

Medical Writing Coordinator/Publisher III - Remote

AbbVie

22 weeks ago

The Medical Writing Coordinator/Publisher III manages document publishing and quality assurance for clinical and regulatory documents.

USA
Full-time
Writing
$107,458.00 - $157,500.00/year

E.T

Translational PK/PD Modeling Consultant - Remote

Entrada Therapeutics

23 weeks ago

Entrada Therapeutics is seeking a Translational PK/PD Modeling Consultant to advance Ocular research and develop PK/PD models.

USA
Contract
All others

E.L.C

Clinical Development Scientist - Gene Therapy - Remote

Eli Lilly Canada

25 weeks ago

Join Lilly as a Clinical Development Scientist to manage clinical supplies and support global clinical programs in gene therapy.

USA
Full-time
All others
$63,000 - $140,800/year

Neumora

Senior Director/Director, Clinical Scientist - Remote

Neumora

25 weeks ago

Seeking a Senior Director/Director, Clinical Scientist to lead scientific expertise in drug product development at Neumora.

Worldwide
Full-time
All others
219919 - 281275/year