Regulatory associate Work, Jobs (with Salaries)

Associate II, TMF Operations - UK - Remote
Worldwide Clinical Trials —England
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Administrative experience
Regulatory Associate - UK Medicines
Reckitt —Slough
- Data analysis skills
- Communication skills
- Employee assistance programme
- Life insurance
Regulatory Compliance Associate
GoCardless —Leeds
- £46,400 - £69,600 a year
- Communication skills
Associate - Government and Regulatory Relations Policy Coordinator
JPMorganChase —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
12d
Associate, Governance & Oversight Specialist
Janus Henderson —London
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- IT
Clinical Research Associate (CRA)
Aspire Pharma Ltd —Remote
- Monday to Friday
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee assistance programme
13d
Clinical Research Associate
IQVIA —Nottingham
- No degree
- Travel
Clinical Research Associate, South West England
IQVIA —Bath
- Maintenance
- No degree
Associate, Company Secretarial Assistant
Janus Henderson —London
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Microsoft Office
AML Associate
PJT Partners —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quality Assurance Associate
IXICO —London
- Full-time
- Hybrid work
- Computer literacy
- Microsoft Office
- Administrative experience
- Annual leave
- Employee assistance programme
Associate Practitioner, Molecular Pathology Department
Health Services Laboratories (HSL) —London
- Up to £38,005.20 a year
- Full-time
- Annual leave
- Employee assistance programme
3d
Data Analyst - Sustainability
SC Johnson Professional —Denby
- Full-time
- Hybrid work
- SQL
- Bachelor's degree
- Free parking
- Annual leave
Quick apply
Clinical Research Associate II, South West England
IQVIA —Bath
- Maintenance
- No degree
Senior Regulatory Affairs Associate
Simbec-Orion —Remote
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
Regulatory Affairs Associate/Manager
Transpire BIO Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
4d
Associate, Analyst NAA Operations CoE, Audit and Assurance - Permanent/ 12 Month FTC/ Secondment
Deloitte —Cardiff
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
12d
Clinical Research Associate - Freelance
TFS HealthScience —London
- Remote
- Nursing
- English
- Bachelor's degree
Quick apply
2d
KYC Associate
Partners Capital —London
- Microsoft Excel
- Microsoft Outlook
- Microsoft Office
- Life insurance

I want to receive the latest job alerts for regulatory associate

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 associate jobs near

Quality Assurance Associate jobs in London

Regulatory Affairs Manager jobs in London

Regulatory Affairs Specialist jobs in Slough

Data Governance Analyst jobs in London

Regulatory Affairs Specialist jobs in Remote

Clinical Research Associate jobs in Nottingham

Compliance Officer jobs in Leeds

Clinical Research Associate jobs in London

Quality Assurance jobs in Birmingham

Quality Assurance Associate jobs in Derby

Quality Assurance Associate jobs in Slough

Quality Assurance Associate jobs in Manchester

Regulatory Affairs Manager jobs in Slough

Part Time Project Manager jobs in London

Project Manager jobs in Huddersfield

School Facility Manager jobs in London

Cardiac Nurse Specialist jobs in London

Regulatory Affairs Specialist jobs in Newcastle Upon Tyne

Government Affairs Health Pharmaceutical Policy jobs in London

Graduate Regulatory Affairs jobs in London

Associate II, TMF Operations - UK - Remote

Worldwide Clinical Trials -
England

Apply Now

Job details

Full-time

Qualifications

Microsoft Word
Microsoft Excel
Clinical research
Administrative experience
Organisational skills
Communication skills

Full job description

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Records Management Compliance Department does at Worldwide

TMF Operations handles the processing, maintenance and archiving of all essential documents in strict accordance with pertinent Standard Operating Procedures, country-specific regulations, and industry best practices. Throughout Worldwide Clinical Trials, our culture of collaboration and innovation is what propels us in our pursuit of excellence in clinical research and making a meaningful impact on every patient's life. Roles within our TMF Operations department have a global scope, with the opportunity to regularly collaborate with members of the Worldwide Project Team.

What you will do

Fulfil the "TMF Approver" and/or "TMF QC Reviewer" roles as defined by the relevant Standard Operation Procedure(s) (SOP) and working practices.

Process, review, and resolve rejected Trial Master File (TMF) documents, for complex studies or Sponsor portfolio of studies both in an electronic and hard copy format.

Prepare periodic TMF Quality Control checklists for review by Project Team review.

Perform periodic TMF Quality Control to ensure adherence to regulatory, ICH GCP, Sponsor, and industry best practices.

Work with a variety of Electronic Document Management and electronic TMF Systems to review, classify and process Essential Documents

What you will bring to the role

Possess data collection, indexing and editing skills, including ability to adhere to standardized document naming conventions

Possess excellent written and verbal communication skills to clearly and concisely present information

Display strong interpersonal skills in a fast-paced, deadline oriented, rapidly changing environment

Handle multiple, highly detailed tasks with exceptional accuracy. Demonstrate strong planning and organizational skills

Demonstrate proficiency in Microsoft Word and Excel

Develop proficiency in use of an electronic document repository or eTMF. General understanding of clinical research principles and processes

Your experience

Minimum 6 months of administrative experience, preferably but not strictly in the CRO or Pharma industry

Knowledge of working within a highly regulated industry (desirable)

A strong, long ‑ term interest in administrative ‑ focused work, with close attention to detail and comfort handling routine, process ‑ driven tasks

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law .

Apply Now

Refine Your Search

regulatory associate jobs

Associate II, TMF Operations - UK - Remote

Regulatory Associate - UK Medicines

Regulatory Compliance Associate

Associate - Government and Regulatory Relations Policy Coordinator

Associate, Governance & Oversight Specialist

Clinical Research Associate (CRA)

Clinical Research Associate

Clinical Research Associate, South West England

Associate, Company Secretarial Assistant

AML Associate

Quality Assurance Associate

Associate Practitioner, Molecular Pathology Department

Data Analyst - Sustainability

Clinical Research Associate II, South West England

Senior Regulatory Affairs Associate

Regulatory Affairs Associate/Manager

Drug Safety Associate II

Associate, Analyst NAA Operations CoE, Audit and Assurance - Permanent/ 12 Month FTC/ Secondment

Clinical Research Associate - Freelance

KYC Associate

I want to receive the latest job alerts for regulatory associate

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected