Clinical Trials Associate

Monte Rosa Therapeutics, Inc.; Boston (MA); On-site; USD 65,000 - 95,000; Full time

Job summary

Monte Rosa Therapeutics, Inc. is seeking a motivated Clinical Operations Associate to support planning, startup, maintenance, and closeout of clinical trials. You will collaborate with investigators, site staff, and CRO partners to ensure documentation, data quality, and trial timelines are maintained.

The role emphasizes strong organization, attention to detail, and proactive communication to keep study teams aligned and compliant with ICH/GCP and FDA regulations.

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

Responsibilities

• Contribute to development of study 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)

Skills

ICH/GCP guidelines

FDA regulations

Cross-functional collab

Organizational skills

Time management

eTMF experience

Education

BA/BS degree

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