Similar posts
Clinical Safety Coordinator
This vacancy has now expired. Please see similar roles below...
Proclinical is advertising on behalf of a CRO providing development services to the biotechnology, pharmaceutical and medical device industries. The company is looking for a Clinical Safety Coordinator to join their UK based team, either in London or Stirling.
Job Responsibilities:
- Collecting, processing and tracking serious adverse events (SAE) reports and clinical event documents.
- Generating and tracking study report safety narratives.
- Coordinating safety surveillance activities, such as lab reviews and trend analysis.
- Generating Investigator Safety Letters.
- Assisting in the preparation of clinical safety documents.
Skills and Requirements:
- A bachelor's degree and at least 3 years of clinical safety experience.
- Experience with review final study report narratives by clinical safety managers.
- Experience with drafting complex study-specific plans and documents for assigned studies.
- Experience generating Investigator Safety Letters for Medical Monitor and Sponsor review.
- Experience coordinating complex safety surveillance activities, including successful communication with Medical Monitor and Clinical Safety Manager.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Divya Mistry on +442038141315 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Related jobs
US$180000 - US$210000 per annum + Highly Competitive Salary
Boston, USA
Proclinical is actively seeking a Director of Statistical Programming for a global biotechnology company. This is a permanent role with the opportunity to work remotely.
Highly Competitive
Brussels, Belgium
Proclinical is seeking a Professional Services Resource Manager. This role is pivotal in allocating resources to client projects.
Highly Competitive
Brussels, België
Proclinical are representing a medium sized, global biotech who are expanding rapidly due the significant products that are coming through in our clients pipeline.
Up to US$0.00 per annum + Highly Competitive Salary
Princeton, USA
Proclinical is seeking a talented and motivated Director of CMC for a leading biotechnology company located in Princeton, NJ.
Highly Competitive
Brussels, België
Proclinical has been retained by a cutting edge, biopharmaceutical company to appoint a Global Head of Quality for their commercial manufacturing sites.
Highly Competitive
Valais, Switzerland
Proclinical is seeking an Administrative Assistant to work a 12 month contract.
Highly Competitive Salary
Miami, USA
Proclinical Staffing is seeking an Associate Director, Access & Reimbursement - Oncology to join a global pharmaceutical organization.
Up to US$20 per hour + Highly Competitive Salary
Social Circle, USA
Proclinical Staffing is seeking a Warehouse Clerk to join a global pharmaceutical organization.
Highly Competitive
Leiden, Nederland
Proclinical is seeking a Senior Clinical Scientist to join our team. This role is integral to our development organization as we prepare to start clinical development of our Axiomer pipeline.
Highly Competitive Salary
Middletown, USA
Proclinical Staffing is seeking an Operations Manager, Chemical Manufacturing to join a leading healthcare organization.