Regulatory affairs specialist Work, Jobs in Remote (with Salaries)

Senior Regulatory Affairs Associate
Simbec-Orion —Remote
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
Scientific Marketing Specialist- Protein Diagnostics
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Marketing
- English
- Project management
Clinical Sales Specialist
Sol-Millennium Medical —Remote
- Full-time
- Remote
- Nursing
- Sales
- Analysis skills
Quick apply
Pharmaceutical Graphic Designer
Alvotech —Remote
- Full-time
- Remote
- English
- Bachelor's degree
- Organisational skills
Medical Science Liaison
Palvella Therapeutics —Field Based
- Doctoral degree
- Travel
- Leadership
8d
Neurovascular Product Marketing Manager for UK, Benelux & Nordics (m/f/d) - based in the UK
Penumbra —Remote
- Remote
- English
- Analysis skills
- Driving
- Employee stock purchase plan
- Annual leave

Other jobs to consider

Find your next job by exploring related positions.

Senior Regulatory Affairs Associate
Simbec-Orion —Remote
We are looking for a Senior Regulatory Affairs Associate to join our Regulatory Affairs & Technical Writing team where you will be responsible for the…
Regulatory Affairs Consultant - CMC vax/bio (home or office based)
Parexel —Remote
Coordinate submission preparation with various departments including manufacturing, supply chain, quality control and quality assurance, and other regulatory…

I want to receive the latest job alerts for regulatory affairs specialist in remote

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

regulatory affairs specialist jobs near remote

Senior Regulatory Affairs Associate

Simbec-Orion -
Remote

Apply Now

Job details

Permanent | Full-time

Qualifications

Doctoral degree
English
Master's degree
Business development
Bachelor's degree

Full job description

Our Mission:

Our passion for improving patients’ lives motivates us to apply our skills, experience and knowledge to advance medicine.

We achieve this through flexible, innovative, high-quality solutions for our clients, delivered with integrity.

The Role:

We are looking for a Senior Regulatory Affairs Associate to join our Regulatory Affairs & Technical Writing team where you will be responsible for the coordination of Global Clinical Trial applications of new and established medical products and devices, ensuring that applications are conducted in accordance with the latest ICH and Regulatory guidelines. You will ensure that submission documentation is submitted in a timely manner and that the client, operational team and Regulatory Senior Management are kept fully informed of all aspects of the project.

Key Accountabilities:

Act as the Regulatory Lead for designated complex global and early phase clinical trials.
Prepare, review and submit clinical trial applications to Regulatory Authorities, Ethics Committees and any other required regulatory authority.
Assist in producing investigator brochures, protocols, IMPDs and other supporting regulatory documentation.
Prepare Patient Information and Consent Documents and other patient facing documentation.
Support Regulatory Affairs department in maintaining awareness and compliance of current local, national, regional and harmonised guidance and requirements for the format, content, and control of all types of regulatory and ethics procedures and submissions.
Assist Project Managers with month end financial reporting on their projects.
Supervise and mentor less experienced Regulatory Affairs team members.
Perform other duties as assigned by Regulatory Affairs & Technical Writing management team such as developing and writing SOP’s, assisting in Business Development activities etc.

Skills Required:

ESSENTIAL

Bachelor's degree within Science or medical field or equivalent
Extensive experience in submitting clinical trial applications globally to the relevant Regulatory Authorities and Ethics Committees.
Extensive experience and understanding of ICH-GCP.
In depth experience with the EU Directive and National Requirements for clinical trials.
Experience in project reporting and liaising with multiple stakeholders, including clients and internal operational teams.
Excellent command of the English language (written and oral) as well as local language where applicable
Excellent analytical, planning, investigative and problem-solving skills

DESIRABLE

Advanced degree (Masters, PhD) or equivalent
Experience in Clinical Trial submission management of international clinical studies
Extensive experience of working with regulatory agencies.
Understanding of pharmaceutical/drug manufacturing in terms of development, manufacturing and quality.
Fluent in another European language

About Us:

Simbec-Orion is a responsive and agile full-service CRO, delivering studies from first in man through to Phase III. Our experts leverage wide therapeutic experience and specialist expertise to execute a comprehensive portfolio of trials. We are perfectly structured to provide full-service clinical development solutions for small and mid-size drug developers, headed up by a centralised leadership team.

With a focus on tailormade and scalable solutions, we adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients’ lives.

Apply Now

Refine Your Search

regulatory affairs specialist jobs in remote

Senior Regulatory Affairs Associate

Scientific Marketing Specialist- Protein Diagnostics

Clinical Sales Specialist

Pharmaceutical Graphic Designer

Medical Science Liaison

Neurovascular Product Marketing Manager for UK, Benelux & Nordics (m/f/d) - based in the UK

Other jobs to consider

I want to receive the latest job alerts for regulatory affairs specialist in remote

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected