Remote CRA II–III: Impactful Trials & Fast Growth

Optimapharm; Philadelphia (Philadelphia County); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Health insurance

Pension plan

Training & development

Well-being initiatives

Career progression

Job summary

Optimapharm is seeking a CRA II/III to advance clinical research in a remote US role. You will perform site visits, monitor trials, review data, and manage budgets, with a focus on quality and regulatory compliance.

We value independence, strong communication, and the ability to work in a matrix team. Prior ICH GCP knowledge and 2+ years of monitoring experience are required for this role at Optimapharm.

Qualifications

• Bachelor's or higher in life sciences or healthcare field.
• Two+ years of independent clinical trial monitoring experience.
• Strong knowledge of ICH GCP and regulatory requirements.
• Proficient computer skills and data interpretation ability.
• Excellent written and verbal communication; good negotiation skills.

Responsibilities

• Perform routine site visits (pre-study, initiation, interim, closeout) independently.
• Manage sites through regular contact to ensure enrollment and protocol compliance.
• Review CRFs, generate queries, and resolve data issues per guidelines.
• Identify risks and training opportunities for site personnel.
• Prepare CAPA plans and follow up until resolution.
• Assist with EC submissions, document translation, and supervisor tasks.
• Negotiate study budgets and assist with site contracts.
• Administer site payments per project instructions.

Skills

ICH GCP

Trial monitoring

Regulatory knowledge

Computer skills

Data interpretation

Communication

Interpersonal skills

Independence

Matrix environment

Driver's license

Education

University degree in life sciences

Nursing or healthcare degree

Healthcare-related education

Job description

Optimapharm is seeking a CRA II/III to advance clinical research in a remote US role. You will perform site visits, monitor trials, review data, and manage budgets, with a focus on quality and regulatory compliance.

We value independence, strong communication, and the ability to work in a matrix team. Prior ICH GCP knowledge and 2+ years of monitoring experience are required for this role at Optimapharm.