Senior Clinical Research Associate
Posted Aug 20
Posted Aug 20
This is a fully remote position, open to applicants in Florida, +2 more states.
• Identify, select, initiate, and conclude investigational sites for phase II-IV clinical trials.
• Collaborate within a large-scale, fast-paced environment alongside a team of Clinical Research Associates (CRAs).
• Ensure compliance with relevant regulations and ICH-GCP standards.
• Independently and proactively set up and monitor studies.
• Complete reports and manage documentation effectively.
• Submit protocol and consent documents for ethics/IRB approval.
• Prepare necessary regulatory submissions.
• Address and manage sponsor-generated queries.
• Take accountability for the cost efficiency of studies.
• Prepare and assess study documentation and feasibility studies for new proposals.
• Potentially assist in the training and mentoring of fellow CRAs.
• Provide support for sponsor-dedicated Dermatology and Rare Disease trials.
• A minimum of 18 months of monitoring experience in phase I-III trials as a CRA.
• A college degree in medicine, science, or a related field.
• Prior monitoring experience in medium-sized studies, including study start-up and close-out processes.
• Familiarity with ICH-GCP guidelines.
• Capability to review and assess medical data.
• Exceptional written and verbal communication skills in both German and English.
• Ability to meet tight deadlines.
• Willingness to travel at least 60% of the time, both internationally and domestically, by air and car.
• A valid driving license.
• Legal authorization to work in the country where the position is located.
• Competitive salary packages.
• Annual performance bonuses.
• Health-related benefits for employees and their families.
• Medical, dental, and vision coverage where applicable.
• Attractive retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programs and wellbeing resources.
• Opportunities for learning and development through structured training and career pathways.
• An inclusive and accessible workplace.
• Reasonable accommodations during the recruitment process.
Worldwide Clinical Trials
Emerald Clinical
Everest Clinical Research
Everest Clinical Research
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