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Jobs 1 - 10 of 78

Ctd jobs

Baltic Training Services |
Sale, England
- 8h ago
Something that is both effective and efficient. Founded in 2010, they are proud have worked with some industry leading brands such as Primark, Jewson, PGL, CTD and many more. Reporting into the...
Real Resourcing |
Berkshire, England
- 8h ago
Manage comprehensive regulatory submission processes to support regulatory strategy and timely quality regulatory submissions (CTAs, INDs, MAAs (CTD e CTD), NDAs, PSURs, variations). Interface...
Watton Hall Limited |
Staddlebridge
- 8h ago
Good understanding of the Drug Development process. Knowledge of international guidelines and requirements. Previous Involvement in preparation of CTD Modules and IMPD IND IB preclinical...
Quality Start |
(Unspecified city), England
- 8h ago
This will include regulatory submission requirements, eCTD and NEES submission documents, authoring, review and approval of CTD components for Module 3, write and review Quality Expert...
Hays Life Sciences |
(Unspecified city), England
- 8h ago
As a Regulatory Publishing Specialist you will also use electronic CTD publishing software, working specifically to regulations and guidelines to ensure eSubmissions compliance, whilst...
PAREXEL |
Uxbridge, England
- 5d ago
Qualifications. Clinical research medical writing experience. Experience in writing multiple clinical study reports, and either CTD documents or study protocols. Preferably experience in a...
PAREXEL |
Uxbridge, England
- 15d ago
Qualifications. Clinical research medical writing experience. Experience in writing multiple clinical study reports, and either CTD documents or study protocols. Preferably experience in a...
Teva Pharmaceutical |
Harlow, England
- 13d ago
Main Responsibilities. The candidate shall have experience with electronic CTD (eCTD) publishing... Candidate will prepare submissions and applications in the Common Technical Document (CTD) in electronic...
Real Resourcing |
Berkshire, England
- 8h ago
Manage comprehensive regulatory submission processes to support regulatory strategy and timely quality regulatory submissions (CTAs, INDs, MAAs (CTD e CTD), NDAs, PSURs, variations). Interface...
QuintilesIMS |
(Unspecified city)
- 12d ago
Extensive experience working as the Lead Medical Writer on protocol and CSR projects in Phase II and III. Experience in authoring CTD modules 2.5, 2.7.3, or 2.7.4, and or in leading coordinating...
Barrington James Ltd |
Staddlebridge
- 1d ago
Clinical Study Reports. Protocols, Clinical Summaries in CTD format, Investigator Brochures, scientific publications Experience interacting directly with clients or authors of the documents and...
Turner Regulatory Recruitment ltd |
Belfast
- 3d ago
This highly successful Consumer Care Organization, seeks a Regulatory Officer within an expanding Team. ideally, you will be seasoned in the following processes. CTD Dossiers for MAA's (all...
COVANCE |
Leeds, England
- 1d ago
To work directly with client Medical Statistical teams to plan and develop CSRs and with guidance from Senior Writing staff, higher level regulatory submissions (e.g., CTD Summaries...
Barrington James Ltd |
London
- 8h ago
Input into the clinical study protocol and Clinical Study Report and Clinical sections of the CTD for regulatory submissions, while working collaboratively with the cross functional Clinical...
Inc Research Uk Limited |
(Unspecified city)
- 8h ago
Preparing and reviewing regulatory submissions (such as INDs, NDAs, IMPDs, CTD, eCTDs), reviewing clinical site regulatory documents, assisting executive management with the administration of...
Barrington James Ltd |
Staddlebridge
- 1d ago
Clinical Study Reports. Protocols, Clinical Summaries in CTD format, Investigator Brochures, scientific publications Experience interacting directly with clients or authors of the documents and...

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