Title: Join Our Team as a Clinical Trial Associate in Greater Boston!

Introduction:

Our client, a leading mid-sized bio-pharmaceutical company specializing in clinical trials is seeking to hire an experienced and detail-oriented Clinical Trial Associate for their office located in Greater Boston. As the selected candidate, you will be responsible for supporting clinical trial activities to ensure that they are completed on time while maintaining high-quality standards. This is a contract to hire opportunity!

Responsibilities:

* Support the Clinical Team in the management of clinical trial documents and site start-up activities. Ensure that all trial-related documents are properly managed in the Trial Master File (TMF), reviewing them for completeness, accuracy, and compliance with protocols, applicable regulations, and standard operating procedures.
* Participate in vendor and internal study team meetings. Responsibilities include drafting agendas, minutes, and other meeting materials as needed to ensure clear communication and documentation.
* Provide administrative support for contract processing, document formatting, and publishing as needed. Perform quality checks and follow-up on the resolution of open issues to ensure compliance with required systems and documentation across the cross-functional study team.
* Documentation Review and Preparation: Assist in the review and preparation of both external and internal documentation for assigned clinical trials.

Required Experience:

* Location: Must be located in the New England area.
* Education: Bachelor's degree or equivalent training.
* Work Experience: At least 2 years of related work experience in clinical trial support, document coordination in a pharmaceutical or CRO environment.
* Regulatory Knowledge: Working knowledge of ICH/GCP regulations and clinical protocols.
* Technical Skills: Demonstrated computer aptitude in MS Office Suite and other systems. Good working knowledge of management and oversight of eTMFs. Experience with Veeva Vault is highly desired.
* Flexibility: Ability to accommodate a flexible work schedule according to clinical trial priorities.

Don't miss out on this fantastic opportunity! Apply today by submitting your resume/CV detailing relevant education/experience history via our application portal.

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real, please visit www.realstaffing.com