Senior Clinical Research Associate - US

Optimapharm; Boston (MA); Remote; USD 80,000 - 120,000; Full time

Job summary

A leading global CRO, Optimapharm, is seeking a Senior Clinical Research Associate to join their expanding Clinical Operations team in the US. This home-based role involves independent site visits, compliance management, and requires a degree in medical or life sciences along with significant clinical trial experience. The company offers a competitive salary, comprehensive benefits, and opportunities for career growth.

Benefits

Support for work-life balance

Healthy culture

Competitive salary and PTO

Health, vision, dental insurance

Comprehensive pension plan

Employee engagement and well-being programs

Training and development

Fast career progression

Qualifications

• At least 3+ years of independent clinical trial monitoring experience.
• Strong knowledge of ICH GCP Guidelines and regulatory requirements.

Responsibilities

• Perform routine site visits independently.
• Manage site compliance and enrollment.
• Negotiate study budgets and assist with site contracts.

Skills

Communication

Interpersonal skills

Negotiation skills

Computer skills

Ability to analyze scientific journals

Proactive work style

Ability to work in a matrix environment

Education

University degree in medical or life sciences

Job description

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Location: home-based

Remote preferred locations: Texas, Florida, Arkansas, Oklahoma

Who we are

Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.

Our key priorities are the well-being of our people, consistent quality delivery to our clients, and sustainable growth.

With 26 offices in over 40 countries, established nearly 20 years ago, we leverage our experience and flexible approach to secure high client trust and growth.

Join our expanding Clinical Operations team in the US as a Senior CRA and contribute to transforming clinical research and improving lives worldwide.

What we offer

• Growing, successful company
• Support for work-life balance
• Healthy culture
• Experienced clinical research team
• Competitive salary and PTO
• Health, vision, dental insurance
• Comprehensive pension plan
• Employee engagement and well-being programs
• Training and development
• Fast career progression

Who are we looking for?

Qualifications and Experience

• University degree in medical or life sciences, nursing, or relevant healthcare field
• At least 3+ years of independent clinical trial monitoring experience
• Strong knowledge of ICH GCP Guidelines and regulatory requirements
• Proficiency in computer skills
• Ability to analyze scientific journals
• Excellent communication skills
• Interpersonal and negotiation skills
• Independent, proactive work style
• Ability to work effectively in a matrix environment
• Valid driver’s license

Your responsibilities

• Perform routine site visits independently
• Manage site compliance and enrollment
• Review CRFs and resolve queries
• Identify risks and retraining needs
• Prepare CAPA plans and follow-up
• Handle documentation for EC submissions and translations
• Negotiate study budgets and assist with site contracts
• Administer site payments

Join our team for growth and career development. Please send your CV. Only shortlisted candidates will be contacted. Compensation is competitive and based on experience.

Disclaimer: Unsolicited CVs from recruitment agencies will not be considered. We collaborate only with selected recruitment partners.