Quality Manager - Environmental Laboratory HA 2622 A fantastic opportunity has arisen for a Quality Manager to join a busy environmental laboratory who specialise in delivering expert analytical services for a variety of clients. Qualifications: For this position it is anticipated that the successful Quality Manager will have a BSc / MSc (or equivalent) in an appropriate chemistry / analytical discipline. <br ...
Job Description Main purpose of the job: To provide specialist care focused scientific and technical support to European medical affairs and marketing activities and to support/prepare the launch activities for other products To Design, implement and manage sponsored Phase IV studies and data generation within European markets and coordinate affiliate generated data review and approval process (IIT). <br /...
You will provide technical assistance to the manufacturing team with regard to new launches and changes to existing products or processes. Prepare and maintain manufacturing instructions to incorporate best practice for both our pharmaceutical and toiletry products. The ideal background for this role will have a science degree, with research, development and formulation of cosmetic, beauty, personal care, skin care, sun c...
Job Description Responsible for the quality and regulatory compliance for studies in Start-up Phase. Perform SSU Project Team Management activities, coordinate the efforts of SSU Team Members and maintain clear client and internal team communication, process documentation, and compliance with Good Clinical Practices and procedures set forth by The Company and its clients. • Organizes efforts of team members assig...
Job Purpose The Chemist is a member of a team within Analytical Science (AS) and is involved in executing analytical programs assigned to Devlab. Analytical assignments involve formulated and unformulated pharmaceutical substances to be used in preclinical and clinical studies. Primary Activities Execute validation of analytical methods. Apply analytical methods and simple analyti...
Job Description Responsible for the successful planning, implementation and execution of contracted clinical activity. Assures the accurate transfer of contracts from proposal through project completion. Functionally responsible for all team members throughout the duration of each clinical trial. Assures clear client communication, process documentation, and compliance with Good Clinical Practices and proc...
Job Description Experience required: (1) CDISC, including SDTM. (2) Minimum 5 years working in pharmaceutical or CRO environment. (3) Early phase clinical trials. (4) SAS programming (not just point-and-click programming in Enterprise Guide). (5) Ability to explain what validation involves, and why it is necessary. Job description: (1) SAS program developmen...
Pharmacovigilance Associate to join an expanding company in Hatfield, Hertfordshire. As Pharmacovigilance Associate you will be a Life Science graduate of Healthcare professional. The Pharmacovigilance Associate will be offered a salary in the region of £25,000 + benefits. Duties and Responsibilities: Evaluate and process ICSRs (Individual Case Study Reports) including duplicate...
Pharmacovigilance Associate to join an expanding company in Hatfield, Hertfordshire. As Pharmacovigilance Associate you will be a Life Science graduate of Healthcare professional. The Pharmacovigilance Associate will be offered a salary in the region of £25,000 + benefits. Duties and Responsibilities: Evaluate and process ICSRs (Individual Case Study Reports) including duplica...
Good afternoon ladies and gentlemen :-) I am putting my UK hat back on for a few days and am looking to hear from those of you interested in the following Freelance roles: 1) A candidate experienced in the Regulatory requirements of the UK and ideally of other EU countries. IRAS, submissions and documents knowledge are essential for this office based position in our Stevenage, Hertfordshire, office. Can you hit the g...
Good afternoon ladies and gentlemen :-) I am putting my UK hat back on for a few days and am looking to hear from those of you interested in the following Freelance roles: 1) A candidate experienced in the Regulatory requirements of the UK and ideally of other EU countries. IRAS, submissions and documents knowledge are essential for this office based position in our Stevenage, Hertfordshire, office. Can you h...
Good afternoon ladies and gentlemen :-) I am putting my UK hat back on for a few days and am looking to hear from those of you interested in the following Freelance roles: 1) A candidate experienced in the Regulatory requirements of the UK and ideally of other EU countries. IRAS, submissions and documents knowledge are essential for this office based position in our Stevenage, Hertfordshire, office. Can you h...
Good afternoon ladies and gentlemen :-) I am putting my UK hat back on for a few days and am looking to hear from those of you interested in the following Freelance roles: 1) A candidate experienced in the Regulatory requirements of the UK and ideally of other EU countries. IRAS, submissions and documents knowledge are essential for this office based position in our Stevenage, Hertfordshire, office. Can you hit the g...
Good afternoon ladies and gentlemen :-) I am putting my UK hat back on for a few days and am looking to hear from those of you interested in the following Freelance roles: 1) A candidate experienced in the Regulatory requirements of the UK and ideally of other EU countries. IRAS, submissions and documents knowledge are essential for this office based position in our Stevenage, Hertfordshire, office. Can you hit the g...
