Regulatory Associate

Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant)Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £22-25 per hour PAYE (inside IR35)We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulatory Consultant to join on a 12-month contract basis. This role will be sat in the core regulatory...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation and feedback gap...

Associate Manager, Clinical Trials Regulatory Management (m/w/d) - Home-based, Europe page is loaded Associate Manager, Clinical Trials Regulatory Management (m/w/d) - Home-based, Europe Apply locations Reading, Berkshire, United Kingdom Belgrade, Serbia Solna, Sweden Vienna, Austria Warsaw, Poland time type Full time posted on Posted 7 Days Ago job...

DATA PROTECTION ASSOCIATE - HYBRID - GLASGOW/READING Job Title: DATA PROTECTION ASSOCIATE - HYBRID - GLASGOW/READING DATA PROTECTION ASSOCIATE - HYBRID - GLASGOW/READING Data Protection Associate Glasgow or Green Park Reading (2 days/week in office, flex on days) Contract: 6 Months As part of the Data Protection team, the Data Protection...

**Data Protection Associate** **Glasgow or Reading** **Hybrid working (2 days/week in office)** **06 months contract** As part of the Data Protection team, the Data Protection Associate will provide support to facilitate client's compliance framework, including policies, processes, procedures and controls, in place to operate in line with its legal and...

Data Protection Associate / DSAR Specialist - required for leading mobile telecoms company. Role can be based in Reading or Glasgow. Hybrid working - 2 days/week in the office DPA Data Protection Associate with strong DSARs experience - asap start - 6 month contract Company Description As part of the Data Protection team, the Data Protection...

Data Protection AssociateGlasgow or Reading Hybrid working (2 days/week in office)06 months contract As part of the Data Protection team, the Data Protection Associate will provide support to facilitate client's compliance framework, including policies, processes, procedures and controls, in place to operate in line with its legal and regulatory obligations...

Data Protection Associate / DSAR Specialist - required for leading mobile telecoms company. Role can be based in Reading or Glasgow. Hybrid working - 2 days/week in the office DPA Data Protection Associate with strong DSARs experience - asap start - 6 month contract Company DescriptionAs part of the Data Protection team, the Data Protection Associate will...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK Join us on our exciting journey! Remote/Hybrid/Office based working options. Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! As Clinical Research Associate you will be responsible perform monitoring and site management work...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK Join us on our exciting journey! Remote/Hybrid/Office based working options. Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! As Clinical Research Associate you will be responsible perform monitoring and site management work...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK Remote/Hybrid/Office based working options. Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! As Clinical Research Associate you will be responsible perform monitoring and site management work to ensure that sites are conducting...

Data Protection Associate Hybrid working (2 days/week in office) 06 months contract As part of the Data Protection team, the Data Protection Associate will provide support to facilitate client's compliance framework, including policies, processes, procedures and controls, in place to operate in line with its legal and regulatory obligations in relation...

Data Protection Associate Glasgow or Reading Hybrid working (2 days/week in office) 06 months contract As part of the Data Protection team, the Data Protection Associate will provide support to facilitate client's compliance framework, including policies, processes, procedures and controls, in place to operate in line with its legal and regulatory...

**Company Overview** Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients. As a...

Data Protection Associate / DSAR Specialist - required for leading mobile telecoms company. Role can be based in Reading or Glasgow. Hybrid working - 2 days/week in the office DPA Data Protection Associate with strong DSARs experience - asap start - 6 month contract Company Description As part of the Data Protection team, the Data Protection Associate...

join us on our mission to drive healthcare forward! We are recruiting for a Senior Clinical Research Associate to assist our sponsor’s Early Development team (phase 1). This is a fully remote position (open to candidates anywhere in the UK) with travel to sites. Professional development - resources that promote your career growth and programs to help...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation...

A UK law firm that are renowned for providing career development, are currently looking for a compliance Manager to join their team to help to enhance and develop their compliance programme. In this role you will be responsible for the firm's compliance and regulatory commitments and processes. You will work closely and meet regularly with the Managing...