Clinical Trials Associate
monterosatx· Clinical Operations
About this role
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
Frequently Asked Questions
What is the salary for the Clinical Trials Associate role at monterosatx?
The listed salary for this Clinical Trials Associate position at monterosatx is USD 70K–100K/yr. This is an FULL TIME role.
Where is the Clinical Trials Associate position at monterosatx located?
This Clinical Trials Associate role at monterosatx is based in Boston, MA, US. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Clinical Trials Associate role at monterosatx full-time or part-time?
This is listed as a FULL TIME position. It is posted as a Clinical Trials Associate role in the Clinical Operations department at monterosatx.
Which team or department does the Clinical Trials Associate at monterosatx belong to?
This Clinical Trials Associate position is part of the Clinical Operations department at monterosatx. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Clinical Trials Associate position at monterosatx?
Click the "Apply Now" button on this page. You will be redirected to monterosatx's official application portal hosted on icims where you can submit your application directly.
When was the Clinical Trials Associate job at monterosatx posted?
This Clinical Trials Associate position at monterosatx was posted on Sep 18, 2026. Apply as soon as possible — early applications are often reviewed first.
Clinical Trials Associate
monterosatx · 💰 USD 70K–100K/yr
You'll be redirected to monterosatx's official application page on icims.