DUTIES AND RESPONSIBILITIES (NOT LIMITED) Ensuring that a company’s products comply with the regulations of the MHRA. Provides regulatory information, guidance and support to the R&D, Commercial, Clinical and Quality functions with respect to the development of company products. Responsible for the timely management, preparation, submission and follow up of regulatory submissions to Competen...
Job Description The main role of this data manager post will be to support the CRF in the running of the in-house, national and international clinical trials. The post holder will be asked to provide support to particular studies as and when the need arises in that area. Responsibilities include creation and maintenance of files for clinical trials, collection of trial data and completion of case report fo...
DUTIES AND RESPONSIBILITIES (NOT LIMITED) Knowledge and use of the Pharmacovigilance database for processing of Adverse Events and Adverse Drug Reactions. Literature searches and obtaining literature articles and reviews. Submission of AEs and ADRs in the appropriate format to the Regulatory bodies, in compliance with the statutory timelines. Organisation of all cases into a com...
WORKING RELATIONSHIPS: Accountable to the New Drug Development and Scientific Affairs Manager on a day to day basis. DUTIES AND RESPONSIBILITIES (NOT LIMITED) Clinical trial officer is responsible for the co-ordination, tracking and documentation of clinical trial activities. The CTO will also provide support for the preparation and filing of trial related communications and docume...
This exciting opportunity has arisen for an experienced environmental consultant to join a leading engineering consultancy. Our client is active in all areas of the construction market and provides services throughout the UK, Europe and the UAE. You will be responsible for the management and delivery of environmental impact assessment work in the UK and overseas, assisting in developing a client base and marketing the services of the ...
Title: Associate Director: Ecology Location: London, Birmingham, Bristol or Cardiff Salary: £40k - £50k with excellent benefits Ref: 11174 Job Summary: An opportunity exists for an experienced ecologist to join my client’s ecology team at an Associate Director level. As a senior team member within a highly respected multi-disciplinary engineering company, you wi...
Spanish and/or Italian-speaking Research Analyst- join a well-established growing company based in Central London London £25,000-£40,000- dependant on experience Euro London Appointments is recruiting on behalf of an international Research Company looking for someone to join their small and efficient Research team in the heart of Central London. Responsibilities include: • Thorough and detail...
Cell Culture Technician Evidence of a Hepatitis B vaccination is ESSENTIAL for this role. The Role: A new opportunity has arisen where our client is seeking a Cell Culture Technician located in their London site. The main focus of this role will be to work within the cell culture lab within the translational research team and maintain both the laboratory and the cell lines used in translational researc...
A global instrument vendor is seeking an experienced sales person to lead the sale of their chromatography consumables product range. You will be home based with a sales territory covering East Anglia and the South East Of England. You will be responsible for meeting annual sales targets, maintaining business with key accounts, and identifying new business in expanding scientific markets. The ideal candidate will have experienc...
A global instrument vendor is seeking an experienced sales person to lead the sale of their chromatography consumables product range. You will be home based with a sales territory covering East Anglia and the South East Of England. You will be responsible for meeting annual sales targets, maintaining business with key accounts, and identifying new business in expanding scientific markets. The ideal candidate will have experie...
Job Summary Senior Quality Assurance Auditor is responsible for conducting audits of on-going clinical research and data management projects, as well as assisting with handling other QA program initiatives. Location Any INC Office Core Responsibilities • Conducting and documenting assigned audits of the projects and operational processes in acco...
Our client is a leading pharmaceuticals business, due to rapid growth and expansion we are recruiting for an experienced Regulatory Affair Manager to join the team based in exclusive West London offices. As Regulatory Affairs Manager you will have previous experience and a deep understanding of National Phase procedures. Key responsibilities: Submission of End of Procedure national phase documents for C...
Senior Specifications Technologist – Food – South East England -27.5K My client, a large international manufacturer of sandwiches and prepared foods is currently in the process of recruiting for an experienced Specifications Technologist to be based in there site located in the South East. The ideal candidate for this position should be an experienced Specification Technologist, you should have a strong understanding of the p...
30 jobs matching this search were posted in the last week
Job Summary This is an exciting opportunity to join our growing Site Start Up business unit. At INC Research, we are committed to delivering studies on time and on budget, without compromising data quality. We understand the necessity of ensuring operational excellence right at the outset of any study and with our Trusted Process have been able to reduce both the time and cost to our clients, with the average study st...
We are seeking a QP/QA Manager for a pharmaceutical company in Middlesex. Job Summary: To ensure effective Quality Management Systems are maintained within the Group incorporating all aspects of quality assurance and quality control. The role also ensures effective coordination of the required work flow within the RA department, and that applicable regulatory compliance is strictly maintai...
Senior EIA Specialist - Central London - £25,000 - £30,000 A world renowned engineering consultancy is looking to expand the environmental team in London with a Senior EIA Specialist. Requirements: A successful track record of EIA co-ordination/project management including budget control A thorough understanding of UK legislation, guidelines and planning processes At least 3 years EIA experi...
Ecologist - London - £20,000 - £26,000 A leading ecological consultancy based in London is looking to expand the team with an Ecologist. The ideal Ecologist will have at least 3 years experience in ecological consultancy and hold one or more protected species licences. You will have extensive experience of protected species survey, with bat experience being highly desirable. As an Ecologist you will ...
Job purpose to: To support the Quality team and to provide support to the division on all related matters at the direction of and reporting to the Quality Manager. This will include holding responsibility for key elements of the divisions QMS and Investigation process driving forward continuous improvement and championing quality in all areas. Key Accountabilities Undertak...
Job Summary Provides customer-focused leadership in the execution of the start up of sites in one or multiple Phase II through Phase IV clinical trials across all functional Site Start-Up (SSU) areas. Accountable for the delivery of activation-ready study sites on time, on budget, and in compliance with all applicable regulations. Responsible for managing all site start-up activities from site selection/recommendation thru site-...
Job Summary Our General Medicine Business Unit is hiring INC Research specializes in providing clinical trials services to support global Phase I - Phase IV studies, and we offer deep therapeutic clinical trial expertise across a wide variety of indications, as well as for special populations, such as women and pediatrics. Core Responsibilities We are currently loo...
Job Summary INC Research’s depth of experience and customer-centered approach to our global data management and biostatistics business sets us apart from other CROs, allowing us to provide sound statistical guidance and input at every stage of a product’s development. Our core strength lies in our ability to deliver high-quality data through a process-driven approach founded on Six Sigma principles, resulting in significant time...
Regulatory Affairs Officer My client is a dynamic and successful pharmaceutical company based in North West London involved in the development, manufacturing and distribution of generic pharmaceutical products. You will be responsible for the development and implementation of processes covering the regulatory activities pertaining to issuance and updating of commercial artwork. You will be expected to b...
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Date: 6 days ago
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Wembley, Middlesex
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£50,000 - £65,000 per annum, negotiable, pro-rata, inc benefits
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3 applications
QP/QA Manager - Pharma - Middlesex - Circa 60k Type: Permanent Benefits: 23 days + Bank Holidays, Employee Discount PURPOSE: To ensure effective Quality Management Systems are maintained within the Group incorporating all aspects of quality assurance and quality control. The role also ensures effective coordination of the required work flow within the RA department, and that applicable regulatory compliance is strictl...
You’ll be tasked with creating and implementing a creative strategy for business growth, the objective of which will be to raise and manage funds intended to further the development and offerings of the business. You’ll have exceptional stakeholder relationship skills and the ability to forge new partnerships with international governmental departments and other donors. You’ll be working to create a sophisticated 5 year models for growth. ...
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Date: 6 days ago
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North London, London
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£28,000 - £35,000 per annum, negotiable, pro-rata, inc benefits
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26 applications
PHARMACOVIGILANCE TEAM LEADER - PHARMA - LONDON - 22-28k TYPE: PERMANENT LOCATION: LONDON SALARY: 28-35k dep on experience Reason: Growth & Investment PURPOSE: Responsibility and management of small Pharmacovigilance Team. KEY DUTIES AND RESPONSIBILITIES: Total management of PV team as well as Training of staff memebers. Have knowledge and use of the Pharmacovigilance database ...
