Life Sciences & Technology | Clinical Research & Clinical Affairs
Location: Remote (MA)
Duration: 12 months (chance of extension) – (40/hrs a week)
A Black Diamond client is looking for a senior/mid level TMF Specialist who will be responsible for the overall management and quality maintenance of essential clinical trial and other designated documents, including the set up and maintenance of the Trial Master File (TMF). This individual will have a strong focus on ensuring that routine document management operations are performed with adherence with SOPs and ICH/GCP/regulatory guidelines. This position plays a key role in both paper and electronic TMF system management, by filing, organizing and maintaining paper and/or digital records and coordinating the document management activities performed by third parties, such as vendors, clinical sites, collaborators, as well as other internal and external team members, as required.
eTMF / TMF
Bachelor’s Degree in a scientific discipline
JOB ID# 226948
23 Main St Suite 3 Andover, MA 01810 Call: 800-681-4734 or 978-474-9980 View all locations