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Regulatory Clinical Trials Submission Manager
UNITED KINGDOM, , UNITED KINGDOM
ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions...
Head Of Clinical Data (Healthtech/Clinical Trials)
LONDON, ENGLAND, UNITED KINGDOM
Overview The Clinical Data Lead holds a pivotal role within a Series A healthtech/clinical trials company, requiring a candidate with a medical background. They will spearhead the establishment and management of crucial clinical data contracts with hospitals, both domestically and internationally...
Regulatory Clinical Trials Submission Manager
p ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research...
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Head of Clinical Data (Healthtech/Clinical Trials)
LONDON, ENGLAND, UNITED KINGDOM
Overview The Clinical Data Lead holds a pivotal role within a Series A healthtech/clinical trials company, requiring a candidate with a medical background. They will spearhead the establishment and management of crucial clinical data contracts with hospitals, both domestically and internationally...
Regulatory Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global...
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Associate Director/Senior Manager, Clinical QA (remote)
LONDON, ENGLAND, UNITED KINGDOM
Proclinical is seeking an Associate Director, GCP Quality to contribute to the mission of developing better medicines, faster to work remotely. In this role, you will lead the GCP Quality support for interventional clinical trials, serve as a GCP Quality expert to the business, and establish strong...
Associate Director - Quality Assurance
, , UNITED KINGDOM
...high level specialist expertise to both the A team and key stakeholders in relation to this manufacturing site. The role has responsibility for building and managing a small team of A professionals and creating a strong quality culture on the site. The individual will deputise for...
Director Regulatory Affairs
, , UNITED KINGDOM
...possible approvals of clinical trials and marketing authorization applications. What you will do: As the Regulatory Affairs Director, your duties and responsibilities will include: Managing all aspects of submissions relevant to assigned projects and programs, in accordance with submission and...
GCP QA Manager
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
We are currently working with a pharma organisation who are a growing ecosystem of drug development companies, that provide integrated and specialist operational support for rapidly scaling biotech ventures. They are looking for a GCP QA Manager who will work closely with the Head of Quality and...
Regulatory Specialist
MAIDENHEAD
p strong SRG /strong are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. /p p br br Learn more about the general tasks...
Associate Director/Senior Manager, Clinical QA (remote)
REMOTE
p Proclinical is seeking an Associate Director, GCP Quality to contribute to the mission of developing better medicines, faster to work remotely. In this role, you will lead the GCP Quality support for interventional clinical trials, serve as a GCP Quality expert to the business, and establish...
Regulatory Specialist
MAIDENHEAD, SOUTH EAST ENGLAND
p b SRG /b are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. /p p br /p p b The Role: /b /p p The Regulatory Associate...
Associate Director - Quality Assurance
UNITED KINGDOM, UNITED KINGDOM
...high level specialist expertise to both the A team and key stakeholders in relation to this manufacturing site. /p p The role has responsibility for building and managing a small team of A professionals and creating a strong quality culture on the site. /p p The individual will...
Director Regulatory Affairs
UNITED KINGDOM, UNITED KINGDOM
...possible approvals of clinical trials and marketing authorization applications. /p p br /p p b What you will do: /b /p p As the Regulatory Affairs Director, your duties and responsibilities will include: /p ul li Managing all aspects of submissions relevant to assigned projects and...
Director Regulatory Affairs
...possible approvals of clinical trials and marketing authorization applications. /p p br /p p strong u What you will do: /u /strong /p p As the Regulatory Affairs Director, your duties and responsibilities will include: /p ul li Managing all aspects of submissions relevant to assigned...
GCP QA Manager
OXFORDSHIRE
p We are currently working with a pharma organisation who are a growing ecosystem of drug development companies, that provide integrated and specialist operational support for rapidly scaling biotech ventures. /p p br br Find out exactly what skills, experience, and qualifications you will need...
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Heavy Lift Engineer
£55,000 a year
, GB
...commencing br / Ensure compliance with company Health and Safety policies and procedures, this can include spot checks on project teams br / Utilise our reporting software to accurately record all required docuentation br / Always providing an exceptional level of customer service, while...
Matches: compliance
Automation Engineer
From £35,000 a year
GLASGOW, SCT, GB
...procedures and ensure compliance with both internal and external standards br / Assembly supervision and electrical testing of solution hardware (including functional safety systems) under the guidance of experienced Engineers br / Installation and commissioning of solutions on customer sites br...
Matches: compliance
Automation Engineer
From £35,000 a year
SHEFFIELD, ENG, GB
...procedures and ensure compliance with both internal and external standards br / Assembly supervision and electrical testing of solution hardware (including functional safety systems) under the guidance of experienced Engineers br / Installation and commissioning of solutions on customer sites br...
Matches: compliance
Senior Partner – Farming and Commercial Insurance Business
ELGIN, SCT, GB
...to expert advice and specialist support on everything from policy and increasing membership numbers to marketing and media. In this role you’re supporting the needs of the farming community and opening doors to future business opportunities for your agency. br / br / Rewards and support...
Matches: specialist
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