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Senior Clinical Trial Associate Jobs (NOW HIRING)

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

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 ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

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 ...

PTC Therapeutics

Clinical Trial Associate I

Warren, NJ · On-site

$34.75 - $47.50/hr

The Clinical Trial Associate I (CTA) is a key support role within the Clinical Operations department, contributing to the execution of clinical trials that advance innovative therapies for patients ...

New

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... In collaboration with the Sr. CTA/CTM, develop study specific processes to ensure that necessary ...

Ptc Therapeutics, Inc.

Clinical Trial Associate I

Warren, NJ · On-site

$34.75 - $47.50/hr

The Clinical Trial Associate I (CTA) is a key support role within the Clinical Operations department, contributing to the execution of clinical trials that advance innovative therapies for patients ...

New

Triwill Group

Clinical Trial Associate

San Francisco, CA · On-site

$94 - $115/hr

The Clinical Trial Associate will play a key role in supporting day‑to‑day clinical trial operations across multiple studies. This role is ideal for someone who thrives in a dynamic environment ...

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with ...

Allen Spolden

Clinical Trial Associate

Manhattan, NY · Remote

$55K - $65K/yr

Associate's or Bachelor's degree in a relevant field. * Clinical research experience preferred ... Maintain and organize Trial Master File (TMF) documentation. * Assist with regulatory document ...

Verastem

Clinical Trial Associate

Boston, MA

$36.50 - $49.75/hr

Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with ...

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Senior Clinical Trial Associate information

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How much do senior clinical trial associate jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for senior clinical trial associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a senior clinical trial associate?

To thrive as a Senior Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines (such as GCP and ICH), and typically a bachelor's degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and relevant certifications like SOCRA or ACRP are commonly required. Attention to detail, strong organizational skills, and effective communication set high performers apart in this position. These skills ensure the accurate, compliant, and efficient execution of clinical trials, supporting successful study outcomes and regulatory submissions.

What is the difference between Senior Clinical Trial Associate vs Clinical Trial Associate?

AspectSenior Clinical Trial AssociateClinical Trial Associate
Required CredentialsBachelor's degree, experience in clinical trials, often some certificationBachelor's degree, entry-level experience, may have certification
Work EnvironmentLeads trial activities, mentors junior staff, manages complex tasksSupports trial activities, follows protocols, assists senior staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, biotech firms
Common Search & ComparisonMore experienced, leadership responsibilitiesEntry-level, support role

The main difference between a Senior Clinical Trial Associate and a Clinical Trial Associate lies in experience, responsibilities, and leadership. Senior associates typically lead trial activities and mentor others, while clinical trial associates support trial operations under supervision. Both roles are essential in clinical research and are commonly found in pharmaceutical and biotech industries.

What are some common challenges faced by senior clinical trial associates, and how can they be effectively managed?

Senior Clinical Trial Associates often encounter challenges such as managing multiple studies simultaneously, ensuring compliance with evolving regulatory requirements, and maintaining clear communication across cross-functional teams. Effectively managing these challenges involves strong organizational skills, up-to-date knowledge of regulatory guidelines like GCP and ICH, and proactive collaboration with project managers, data managers, and site coordinators. Utilizing project management tools and regularly scheduled team meetings can also help streamline workflows and address issues promptly.
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Senior Clinical Trial Associate jobs near you
Infographic showing various Senior Clinical Trial Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Associate

Candel Therapeutics

Needham, MA • On-site

$88K - $100K/yr

Full-time

Posted 26 days ago

Job description

  • 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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