Needham, MA · On-site
$88K - $100K/yr
... * Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. * Maintain study-related trackers that will ...
Quick apply
Needham, MA · On-site
$88K - $100K/yr
... * Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. * Maintain study-related trackers that will ...
Needham, MA · On-site
$88K - $100K/yr
... * Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. * Maintain study-related trackers that will ...
Needham, MA · On-site
$88K - $100K/yr
... * Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. * Maintain study-related trackers that will ...
Tomball, TX · On-site
$50 - $70/hr
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
Tomball, TX · On-site
$50 - $70/hr
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
Saint Louis, MO · On-site
The Clinical Trial Assistant (CTA) provides administrative and operational support for clinical ... Maintain study correspondenceAssist with sponsor monitoring visits and auditsCoordinate document ...
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Saint Louis, MO · On-site
The Clinical Trial Assistant (CTA) provides administrative and operational support for clinical ... Maintain study correspondenceAssist with sponsor monitoring visits and auditsCoordinate document ...
San Francisco, CA · On-site
$140 - $170/hr
... SOPs, and Monitoring Plan, as required. * With guidance, may assist in review of protocols ... Relevant clinical trial experience in the pharmaceutical or health care industry. Experience as the ...
New
San Francisco, CA · On-site
$140 - $170/hr
... SOPs, and Monitoring Plan, as required. * With guidance, may assist in review of protocols ... Relevant clinical trial experience in the pharmaceutical or health care industry. Experience as the ...
New
Cambridge, MA · On-site
$75K - $90K/yr
The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... May assist with reviewing monitoring visit reports The CTA II will also perform the following CTA ...
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Cambridge, MA · On-site
$75K - $90K/yr
The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... May assist with reviewing monitoring visit reports The CTA II will also perform the following CTA ...
Boston, MA · On-site
$100K - $125K/yr
... * Assist in developing study-specific feasibilities and participate in site selection ... Liaise with medical monitor and cross functional team members as necessary and in accordance with ...
Boston, MA · On-site
$100K - $125K/yr
... * Assist in developing study-specific feasibilities and participate in site selection ... Liaise with medical monitor and cross functional team members as necessary and in accordance with ...
Needham, MA · On-site
$88 - $100/hr
... * Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. * Maintain study‑related trackers that will ...
Needham, MA · On-site
$88 - $100/hr
... * Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. * Maintain study‑related trackers that will ...
San Francisco, CA · On-site +1
$140K - $170K/yr
The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... SOPs, and Monitoring Plan, as required. * With guidance, may assist in review of protocols ...
San Francisco, CA · On-site +1
$140K - $170K/yr
The Clinical Trial Manager (CTM) is a key member of the Clinical Operations team and will report ... SOPs, and Monitoring Plan, as required. * With guidance, may assist in review of protocols ...
Morrisville, NC · On-site
$90 - $120/hr
The CTM oversees vendor management, monitors subject safety and data collection, and ensures ... readiness. * Assist in developing study documents and tools, including informed consent forms ...
New
Morrisville, NC · On-site
$90 - $120/hr
The CTM oversees vendor management, monitors subject safety and data collection, and ensures ... readiness. * Assist in developing study documents and tools, including informed consent forms ...
New
Cambridge, MA · On-site
Manage the operational aspects of clinical trials (e.g., study management, site monitoring and ... * Assist in Development of and manage the study project plan, including timeline, budget, and ...
Cambridge, MA · On-site
Manage the operational aspects of clinical trials (e.g., study management, site monitoring and ... * Assist in Development of and manage the study project plan, including timeline, budget, and ...
Cambridge, MA · On-site
Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines; provide regular trial status updates and metrics. * Guide trial teams ...
Quick apply
Cambridge, MA · On-site
Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines; provide regular trial status updates and metrics. * Guide trial teams ...
Sunnyvale, CA · On-site
$70K - $94K/yr
The Clinical Trial Assistant will play a key role to provide operational support to coordinate the conduct and management of clinical studies to ensure compliance with Intuitive standard operating ...
Sunnyvale, CA · On-site
$70K - $94K/yr
The Clinical Trial Assistant will play a key role to provide operational support to coordinate the conduct and management of clinical studies to ensure compliance with Intuitive standard operating ...
Boston, MA · Hybrid
$70K - $85K/yr
This Assistant Clinical Research Manager (ACRM) position will work within the Breast Oncology ... Trial Monitoring * Assists CRM with responsibility for data management and compliance for entire ...
Boston, MA · Hybrid
$70K - $85K/yr
This Assistant Clinical Research Manager (ACRM) position will work within the Breast Oncology ... Trial Monitoring * Assists CRM with responsibility for data management and compliance for entire ...
Cambridge, MA · On-site
Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines; provide regular trial status updates and metrics. * Guide trial teams ...
Cambridge, MA · On-site
Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines; provide regular trial status updates and metrics. * Guide trial teams ...
Cambridge, MA · On-site
$112 - $160/hr
Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines; provide regular trial status updates and metrics. * Guide trial teams ...
Cambridge, MA · On-site
$112 - $160/hr
Monitor trial progress, including participant enrollment, clinical data review, sample collection, and adherence to timelines; provide regular trial status updates and metrics. * Guide trial teams ...
Reviewing monitoring reports and other study documentation as required. * Oversight of the collection and management of clinical trial documentation to be filed in the Trial Master File (TMF)
Reviewing monitoring reports and other study documentation as required. * Oversight of the collection and management of clinical trial documentation to be filed in the Trial Master File (TMF)
... SOPs * Assist in preparation and review of clinical trial documentation such as; protocol, informed consent, Investigator Brochure, Clinical Monitoring Plan, Project Plan, Case Report Forms ...
... SOPs * Assist in preparation and review of clinical trial documentation such as; protocol, informed consent, Investigator Brochure, Clinical Monitoring Plan, Project Plan, Case Report Forms ...
Boston, MA · Hybrid
$120K - $150K/yr
... Assist with oversight of CRO and vendor set-up, liaising with CROs to ensure timely study ... Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ...
Boston, MA · Hybrid
$120K - $150K/yr
... Assist with oversight of CRO and vendor set-up, liaising with CROs to ensure timely study ... Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ...
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
... assist investigators with obtaining informed consent and coordinate appointments with the ... clinical trial sites and the staff. * Accountable for coordinating pre-screen data management ...
$11.54 - $16.74
4% of jobs
$16.74 - $21.94
15% of jobs
$24.54 is the 25th percentile. Wages below this are outliers.
$21.94 - $27.14
13% of jobs
$27.14 - $32.34
8% of jobs
The median wage is $35.23 / hr.
$32.34 - $37.54
19% of jobs
$37.54 - $42.74
13% of jobs
$44.83 is the 75th percentile. Wages above this are outliers.
$42.74 - $47.95
10% of jobs
$47.95 - $53.15
5% of jobs
$53.15 - $58.35
11% of jobs
$58.35 - $63.55
1% of jobs
$63.55 - $68.75
1% of jobs
$11
$37
$68
| Aspect | Assistant Clinical Trial Monitor | Clinical Trial Monitor |
|---|---|---|
| Credentials | Often requires a bachelor's degree in life sciences or related field; certifications like SOCRA or ACRP are common | Typically requires similar degrees and certifications, with more experience |
| Work Environment | Supports monitoring activities under supervision, often in office or site settings | Leads monitoring visits, oversees site compliance, and makes independent assessments |
| Responsibilities | Assists with data collection, site communication, and documentation | Performs site visits, verifies data accuracy, and ensures protocol adherence |
The main difference is that the Assistant Clinical Trial Monitor supports and assists in monitoring activities, often under supervision, while the Clinical Trial Monitor takes on more independent responsibilities, leading site visits and ensuring compliance. Both roles require similar credentials and work in comparable environments, but the level of responsibility distinguishes them.
Cities with the most Assistant Clinical Trial Monitor job openings:
The most popular types of Clinical Trial Monitor jobs are:
States with the most job openings for Assistant Clinical Trial Monitor jobs include:
$88K - $100K/yr
Full-time
Re-posted 19 days ago
Location: Hybrid, Needham, MA
Salary: $88k-$100k
Why Work With Us?
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com
Position Summary:
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials. This role includes working on multiple protocols with the potential to cross-train across different oncology indications using a variety of clinical trial databases.
Essential Areas of Responsibility:
Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements.
Participate in reviewing, formatting, and finalizing study-related templates, logs, plans, and manuals and ongoing training of personnel.
Assist in collecting and completing essential study-related activities, including data entry into multiple databases.
Ensure the quality of data submitted from assigned study tasks and timely data submission, including appropriate progress reporting.
Manage imaging vendor and maintain tracking of invoices, sample delivery and recovery from the vendor site.
Assist in the planning and organizing study-specific meetings and write and distribute regular updates.
Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review.
Maintain study-related trackers that will support Clinical Operations and individual studies.
Perform primary review of submitted clinical data, database entry, and source document verification according to established standard operating procedures (SOPs).
participate in the review and verification of data for quality control processes.
Ensure quality in documentation and archiving of clinical data.
Support invoice tracking, purchase order coordination, and budget-related activities for study.
Minimum Education, Experience and Skill Requirements:
Education:
Bachelor’s degree in a health-related discipline or similar.
Experience:
At least 2 years of experience in the clinical research/pharmaceutical/biotech arena and an understanding of clinical research and the requirements of a clinical operations function.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Able to manage multiple projects independently and use varying databases and management systems.
Discretion in handling confidential information.
Knowledge of project management tools and practices and proficiency in using normal office software: Microsoft Word, Excel, and PowerPoint.
Must be authorized to work in US. We cannot provide sponsorships.
*** NOTE: We are not accepting resumes from agencies. ***
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Biotechnology research and development
51 - 200 Employees
Needham Heights, MA, US
1999
