Experience with Trial Master File REQUIRED. Position requires attention to detail. Previous Clinical experience required. Someone with previous medical records experience would make a good fit.
Member of the clinical team responsible for conducting Phase I-IV studies according to Federal Regulations and ICH guidelines. Support clinical team, primarily in tracking, organizing and filing Phase I-IV study documents according to Federal Regulations and ICH guidelines. Assist Clinical Team members in handling data queries, drug inventories, study invoice payments, enrollment tracking, and record reconciliation with site documents. Assists the CRAs with organizing and planning study investigator meetings.
Long Term Contract
About The Fountain Group:
The Fountain Group provides Contingent Labor, Statement-of-Work, and Contingent-to-Permanent resources to clients with an internal/external Contingent Labor Managed Service Program or Clients without a program.
The Fountain Group is committed to the belief that we all share in the responsibility to conduct our businesses in a socially and environmentally responsible manner. We base this on the premise that a company is much more than the products it offers. The effect a company has on the environment, the people and the communities it serves reflects the company.