Senior Clinical Research Associate

Run my Accounts AG; Aliso Viejo (CA); Remote; USD 90,000 - 110,000; Full time

Job summary

A leading company is seeking a Clinical Research Associate to support the planning and monitoring of clinical trials. This remote position requires up to 70% travel to ensure compliance with protocols and regulations, requiring a Bachelor’s degree and relevant experience.

Benefits

Stock options

Comprehensive health, dental, and vision insurance

Generous paid time off

Annual bonus opportunity

Qualifications

• Minimum of 4 years of experience in clinical affairs.
• Knowledge of GCP, FDA/ICH guidelines.
• Ability to travel up to 50-75% domestically.

Responsibilities

• Conduct site monitoring visits to ensure compliance.
• Assist in preparation of trial documents.
• Collaborate with site staff for data entry resolution.

Skills

Communication

Problem-solving

Organizational skills

Education

Bachelor's degree in life sciences, nursing, or related field

Tools

Microsoft Office

Electronic Data Capture systems

Job description

About SpyGlass Pharma:

At SpyGlass Pharma, 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 team of driven professionals with diverse expertise in ophthalmic products and drug delivery. Our accomplished scientists and engineers work alongside a seasoned leadership team with extensive experience in ophthalmology and a history of commercial success. Our unifying mantra, “We create for patients” doesn’t just live on our walls but drives our decision making as we build the company, creating the products, processes and culture that make it happen.

This team has delivered a solid foundation of development and clinical data, enabling over $120 million in funding to date with several top-tier venture partners. We are building confidence in the performance of our lead product going into Phase 3 clinical trials.

Summary:

The Clinical Research Associate (CRA) will be a key member of the Clinical Affairs team, responsible for supporting the planning, execution, and monitoring of clinical trials to ensure compliance with protocols, regulations, and company standards. This role requires strong attention to detail, excellent communication skills, and a proactive approach to clinical trial management.

Please note:This is a U.S. based, remote position that requires regular travel to clinical trial sites across the country (up to 70%). Applicants must be currently authorized to work in the United States and comfortable with a travel-based schedule.

Essential Duties and Responsibilities:

• Conduct site monitoring visits (initiation, routine, and close-out) to ensure compliance with the clinical protocol, GCP, and regulatory requirements.
• Assist in the preparation and review of essential trial documents, such as informed consent forms, case report forms, and investigator brochures.
• Collaborate with site staff to ensure proper documentation, timely data entry, and resolution of data queries.
• Assist in the identification, selection, and training of investigative sites.
• Maintain accurate and complete study files and records in accordance with GCP and company SOPs.
• Monitor study progress to ensure timelines and quality standards are met.
• Report site activities and findings to the Clinical Study Manager and escalate issues as necessary.
• Support regulatory submissions by preparing clinical trial applications and maintaining relevant documentation.
• Work collaboratively with cross-functional teams, including Regulatory Affairs, Quality Assurance, and Project Management, to achieve study objectives.
  

Qualifications Required for Position:

• Bachelor's degree in life sciences, nursing, or a related field.
• Minimum of 4 years of experience in clinical affairs within the pharmaceutical or medical device industry, with a preference on drug and drug/device combination products.
  
• Knowledge of GCP, FDA/ICH guidelines, and clinical trial monitoring practices.
• Strong organizational and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to build strong relationships with investigative sites and internal teams.
• Proficiency in Microsoft Office and electronic data capture (EDC) systems.
• Ability to travel up to 50-75% domestically, as required.

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 [e-mail] and let us know the nature of your request and your contact information.