About this opportunity
Monte Rosa Therapeutics, Inc. lists this Clinical Trials Associate opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Overview
We are seeking an energetic and highly motivated individual to join our Clinical Operations team. This position reports to the Head of Clinical Operations and is an opportunity to significantly contribute to the growth and development of a top-tier Biotech company. The COA position is focused on providing support associated with the planning, start-up, maintenance, and closeout of clinical trials. The ideal candidate will be proactive and detail oriented with a desire to be involved in all aspects of clinical trial execution.
Responsibilities
Contribute to the development of study-related documents (Clinical protocols, ICFs, IBs, monitoring plans, study manuals, etc.)
Partner with Investigators and clinical site staff to ensure optimal Sponsor-Site relationships
Review study-specific essential regulatory document packets prior to site activations
Participate in the ongoing review and cleaning of clinical trial data.
Assist with the management of tracking, logistics and quality operations for biological samples to help ensure that sample inventories are accurate and up to date.
Attend and provide support in meeting scheduling and distribution of meeting agendas/minutes
Review monitoring reports and protocol deviations to help track issues and data trends at sites
Assist with IMP tracking to verify adequate supply at sites and depots.
In conjunction with the CRO, manage submission of documents to and maintenance of the TMF, to ensure continual inspection-readiness
Support the study finance and contract processes for 3rd party vendors (invoice tracking, approval and accruals)
Effectively communicate trial details to ensure that all team members are kept informed
Participate in SOP development and process improvement projects (as necessary)
Qualifications
BA/BS degree required with a minimum of 2 years relevant clinical research experience working at an Investigator Site, Sponsor or Clinical Research Organization.
Working knowledge of ICH/GCP guidelines and FDA regulations
Ability to collaborate effectively with cross functional team members and external partners
Strong organizational and time management skills, including the capacity to work independently and prioritize multiple projects
Experience working with eTMFs strongly preferred
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.