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Clinical Trial Associate Ii Jobs (NOW HIRING)

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$90K - $110K/yr

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma ... * 2 years for CTA, 4 years for Sr CTA, 6 years for Sr CTA2, or 8 years for Principal CTA of ...

Spyglass Pharma

Clinical Trial Associate

Irvine, CA

$35.75 - $48.75/hr

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma ... * 2 years for CTA, 4 years for Sr CTA, 6 years for Sr CTA2, or 8 years for Principal CTA of ...

Olema Oncology

Senior Clinical Trial Associate

Boston, MA · On-site

$36.50 - $49.75/hr

... two pivotal Phase 3 clinical trials. We expect top-line data from OPERA-01, our ongoing Phase 3 ... About the Role >>> Senior Clinical Trial Associate As the Senior Clinical Trial Associate reporting ...

Axsome Therapeutics

Clinical Trial Associate

New York, NY · On-site

$60K - $66K/yr

About This Role Axsome Therapeutics is seeking a Clinical Trial Associate (CTA) that is responsible for supporting the organization to successfully develop and implement clinical trials across its ...

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 ...

Rapport Therapeutics

Sr. Clinical Trial Associate

Boston, MA · On-site

$36.25 - $49.50/hr

As a Senior Clinical Trial Associate, you'll be a key player in keeping our Bipolar Mania studies on track-managing the details, supporting the team, and helping bring innovative treatments to ...

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Clinical Trial Associate Ii information

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

As of Aug 17, 2026, the average hourly pay for clinical trial associate ii 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 roles and responsibilities of a Clinical Trial Associate II?

A Clinical Trial Associate II (CTA II) is responsible for supporting the management and coordination of clinical trials. Their duties typically include maintaining trial documentation, assisting with regulatory submissions, tracking study progress, and ensuring compliance with protocols and regulations. They work closely with clinical research teams, sponsors, and vendors to facilitate trial operations. As a level II associate, they often have more experience and may take on additional responsibilities, such as mentoring junior staff or managing specific aspects of a study. This role is essential for ensuring the smooth and compliant execution of clinical research.

What are some common challenges faced by a Clinical Trial Associate II, and how can they be addressed?

Clinical Trial Associate IIs often manage multiple studies and documentation requirements simultaneously, which can make prioritization and organization challenging. Staying compliant with regulatory guidelines and ensuring accurate, timely data entry are critical responsibilities that require keen attention to detail. Effective communication with cross-functional teams, such as clinical research coordinators and project managers, helps streamline processes and address issues quickly. Utilizing project management tools and proactive planning are essential strategies to meet deadlines and maintain study quality.

What are the key skills and qualifications needed to thrive as a Clinical Trial Associate II, and why are they important?

To thrive as a Clinical Trial Associate II, 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 documentation standards is crucial. Attention to detail, strong organizational skills, and effective communication enable you to manage trial documentation and collaborate with cross-functional teams. These abilities ensure trial integrity, regulatory compliance, and the smooth progression of clinical studies.

What is the difference between Clinical Trial Associate Ii vs Clinical Trial Associate I?

AspectClinical Trial Associate IiClinical Trial Associate I
Required CredentialsBachelor's degree, some experience in clinical trialsBachelor's degree, entry-level experience
Work EnvironmentSupports more complex trials, may handle multiple sitesAssists with basic trial activities, supervised closely
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsSimilar settings, often entry-level roles
Common Search & Comparison IntentUnderstanding role progression, responsibilitiesEntry-level position, learning scope of clinical trials

The Clinical Trial Associate II typically has more experience and handles more complex trial activities compared to the Clinical Trial Associate I. The II role involves supporting multiple sites and managing more responsibilities, while the I is often an entry-level position focused on assisting with basic trial tasks under supervision.

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Clinical Trial Associate

Spyglass Pharma

Aliso Viejo, CA • On-site

$90K - $110K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted yesterday

Job description

About SpyGlass Pharma:
At SpyGlass Pharma (NASDAQ: SGP), we are focused on improving and preserving the vision of patients suffering from chronic eye conditions, while minimizing the impact on their daily lives. We aim to achieve this by developing cutting-edge long-term drug delivery products to address common causes of blindness and getting these products to the patients that need them.
We have built a highly collaborative team with deep expertise across ophthalmology, drug delivery, pharmaceuticals, and medical devices. Our scientists, engineers, and clinical leaders bring decades of experience developing and commercializing breakthrough technologies, united by a shared commitment to patients and our guiding principle: "We create for patients." That mindset shapes how we build our products, our teams, and our culture.
Backed by strong clinical progress, significant funding, and a growing organization, SpyGlass Pharma is entering an exciting stage of growth as we advance our lead program, the SpyGlass BIM-IOL, through Phase 3 clinical development.
Summary:
We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma. The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial. This position has the responsibility of supporting the clinical department in executing and implementing global clinical decisions. This includes responsibility for the clinical team's creation of relevant documents and outputs including feasibility questionnaires, regulatory documents, enrollment reports, data listings, and patient summaries. The CTA will review the investigator brochures, study protocol synopsis, clinical study protocols, top line study data, Clinical Study Report (CSR), clinical sections of regulatory documents and the Annual reports. This position executes, implements, and manages various tasks to assist in the achievement of all activities related to the Clinical development program, including achievement of key program milestones within the planned timelines and budget. The position may interact with multiple levels in the organization, participating in discussions with management and providing clinical updates.
Essential Duties and Responsibilities:
  • Support the Clinical Affairs team to execute tasks throughout the clinical trials.
  • Manage and execute the tasks for the strategic objectives defined by the project team
  • Work with clinical team
    to execute global clinical strategies, programs, and protocols.
  • Provide clinical support to interdisciplinary project teams, aligning with FDA/Regulatory Agency requirements, FDA/ICH guidelines, IRB/IEC requirements, Good Clinical Practices (GCP), and industry best practices.
  • Be aware of clinical issues and help to resolve them.
  • Participate in FDA, Regulatory Agency, IRB/IEC meetings as needed.
  • Review of regulatory submissions, including clinical trial applications, IND, IDE, NDA, PMA, annual reports, CIB updates, meeting packages, technical files/design dossier for FDA and other regulatory agencies as needed.
  • Facilitate regulatory document collection and follow-up with team members, ensuring that all documents and tasks are in accordance with predetermined timelines.
  • Work in a dynamic, matrixed environment by collaborating closely with cross-functional teams, including R&D, Regulatory Affairs, Quality Assurance, and project management teams, while following GCP and industry best practices.
  • Interact and coordinate with R&D staff (CMC and Engineering), vendors, and consultants to ensure compliance to applicable Design Control and pharmaceutical requirements (for drug/device combination products).
  • Learn about clinical trends, changes, and requirements in the pharmaceutical industry, providing recommendations to senior management on regulatory matters.

Qualifications Required for Position:
  • Bachelor's degree in life sciences, healthcare, biomedical engineering, or a related field preferred.
  • 2 years for CTA, 4 years for Sr CTA, 6 years for Sr CTA2, or 8 years for Principal CTA of experience in clinical affairs within the pharmaceutical or medical device industry, with a preference on drug and drug/device combination products. (A commensurate combination of education and experience will be considered.)
  • Some experience in a cross-functional development team/subteam in a clinical development organization
  • Knowledge of GCP and industry best practices with clinical trial management, monitoring, regulatory compliance, data management and statistical reporting.
  • Knowledge of US clinical and regulatory requirements and guidelines for drug and drug/device combination products, including FDA/Regulatory Agency requirements, FDA/ICH guidelines, and IRB/IEC requirements.
  • Awareness of preparing US IND/amendments, annual reports, and briefing books.
  • Awareness of preparing the annual budget forecast and monitor expenditures.
  • Knowledge of the CFR, FDA/ICH guidelines, GxP and cGMP as they pertain to pharmaceutical development and manufacturing.
  • Previous experience conducting clinical studies, meetings, enrollment, and interactions with regulatory agencies.
  • Willingness to learn leadership, communication, and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
  • Awareness of clinical strategy development, investigational product supply, regulatory compliance, and clinical activities for clinical trials of all phases.
  • Ability to work in a fast-paced, dynamic environment and manage multiple projects simultaneously while maintaining attention to detail and quality.

Why SpyGlass Pharma?
  • We are offering a range of $90,000 - $110,000, based on experience and qualifications, along with an Annual Bonus opportunity.
  • Share in our success with stock options, giving you a stake in the company's future.
  • Comprehensive health, dental, and vision insurance plans to keep you and your family healthy and happy, with a variety of plan and coverage options.
  • Generous paid time off, including holidays, vacation days, and personal leave.

SpyGlass Pharma is an Equal Opportunity Employer and participates in E-Verify. SpyGlass Pharma takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status.
SpyGlass Pharma is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to JOBS@SPYGLASSPHARMA.COM and let us know the nature of your request and your contact information.

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