Clinical Research Associate
Alliance for Clinical Trials in Oncology
full-time
Posted on:
Location Type: Hybrid
Location: Boston • Massachusetts • United States
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Tech Stack
About the role
- Assist operations team in supporting the Alliance member sites and escalate site related issues when necessary.
- Send, track, and review study-specific and global feasibility questionnaires.
- Assist with site selection and recruitment by generating site identification reports (e.g., site accrual); collecting, reviewing and tracking site feasibility/credentialing documentation and follow-up on site accruals accordingly.
- Track training information and issue trainings for sites and contacts.
- Collection of essential documents related to study start-up and review IP release packages.
- Prepare for and execute Investigator meetings and other site training programs.
- Assist with creation of start-up plans and templates.
- Ensure proper and timely filing of all relevant study documents into the eTMF on an ongoing basis to ensure compliance with applicable work instructions, SOPs and ICH GCP guidelines and AFT expectations.
- Perform routine review of filing procedures to ensure adherence to current quality guidelines at all times.
- Accurately enter and manage data within the Clinical Trial Management System (CTMS) by: tracking completed training information that could carry over to other studies; maintaining site information and rosters; reviewing monitoring reports to identify deficiencies, reviewing adequacy of issue escalation and issue resolution; and provide feedback to appropriate CRO contacts.
- Participate in co-monitoring activities.
- Communicate with CROs, vendors, and/or study sites as necessary to support the study, which includes monitoring email accounts related to studies.
- Conduct regulatory review of ICF changes and coordinate review by Executive Officer and contracts team
- Coordinate study related meetings; take detailed minutes at meetings on decisions and action items and distribute to the team, as assigned.
- Other related duties as assigned to meet departmental and company objectives.
Requirements
- A minimum of a BA/BS degree is required.
- Degree in a health or science major preferred.
- 2 – 4 years relevant experience in biotech, pharma, and/or CRO, including 1 year of clinical research industry experience.
- Working knowledge of clinical monitoring responsibilities and procedures.
- Previous experience with eTMF, CTMS, and IRT clinical trial systems is strongly preferred.
- Proficient in Microsoft Office Suite, especially Word and Excel.
- Strong organizational skills and ability to prioritize workload to meet tight deadlines in a fast-paced and dynamic work environment.
- Strong interpersonal, written, and verbal communication skills.
- Flexible and adaptable to a small business workplace environment.
Benefits
- 8 weeks of paid time off (including PTO, sick, and holidays) during year one
- Medical, Dental & Vision plans with a 100% employer-paid option for employees
- Tuition reimbursement stipends
- Continuing Education
- 3% employer match for retirement investments
- Annual Employee Performance Bonus Program
- Annual Cost of Living Adjustment
- 50% commuter reimbursement
- Healthy Work/Life balance and flexibility
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical monitoringdata managementsite selectionfeasibility assessmentregulatory reviewstudy start-uptraining coordinationissue escalationquality guidelines adherenceclinical research
Soft Skills
organizational skillscommunication skillsinterpersonal skillstime managementadaptabilityattention to detailteam collaborationproblem-solvingprioritizationmeeting coordination