Project Manager (Clinical Trials)

March 6, 2026

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0 Skip to Content Services About Our Specialization Strategy Drug Safety Regulatory IND Preparation Clinical Strategy Project Management Biostatistics & Programming Site Monitoring Data Management Medical Writing Clinical Expertise Areas of Expertise Oncology Respiratory Endocrinology Radiopharmaceuticals About Our Team Our Philosophy Our Location Our Capabilities Careers Certified Diverse Business Contact Us Services About Our Specialization Strategy Drug Safety Regulatory IND Preparation Clinical Strategy Project Management Biostatistics & Programming Site Monitoring Data Management Medical Writing Clinical Expertise Areas of Expertise Oncology Respiratory Endocrinology Radiopharmaceuticals About Our Team Our Philosophy Our Location Our Capabilities Careers Certified Diverse Business Contact Us Folder: Services Back About Our Specialization Strategy Drug Safety Regulatory IND Preparation Clinical Strategy Project Management Biostatistics & Programming Site Monitoring Data Management Medical Writing Folder: Clinical Expertise Back Areas of Expertise Oncology Respiratory Endocrinology Radiopharmaceuticals Folder: About Back Our Team Our Philosophy Our Location Our Capabilities Careers Certified Diverse Business Contact Us Project Manager (Clinical Trials) Project Manager (Clinical Trials) Position: Full Time Location: Remote Job Duties: • Evaluate and train investigators • Attend investigator meetings • Conduct pre-study initiation visits • Orient site personnel to study protocol and procedures • Perform on-site and remote monitoring activities from study start-up through close-out • Verify accurate transcription of data from source documentation to CRF/EDC • Oversee drug accountability • Ensure regulatory inspection readiness at assigned clinical sites • Perform all duties and responsibilities in adherence to protocols, FDA regulations, ICH/GCP guidelines, and company / client SOPs • Minimal travel may be required, based on study specifications • Perform other related duties as needed Knowledge & Skills: • Extensive knowledge of FDA regulations and GCPs • Computer proficient with EDC experience • Detail oriented • Excellent verbal and written communication skills • Ability to work independently with minimal supervision • Ability to proactively identify issues that may impact enrollment and recruitment timelines Education and Experience: • BS/BA in Life Science or Nursing (or equivalent foreign education / experience) required • Minimum of 3 years CRA experience within the pharmaceutical or biotechnology industry • This position can be contract, full-time, or part-time. To apply, send resume and cover letter to hr@clinsmart.com with subject line "Project Manager". Contact Email : info@clinsmart.com Phone : + 1 (215) 623-9900 Corporate 642 Newtown Yardley Road Suite 200 Newtown, PA, 18940, USA Apply tot his job

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