Source Job

United States

  • Create, maintain, and control accurate versions of source documents for clinical trials following GCP and 21 CFR Part 11.
  • Design e-Source and paper source templates based on protocol reviews and coordinate review and update processes.
  • Manage version control, communication with site staff, and ensure source documents record all required trial data.

Clinical Research Excel Written Communication

8 jobs similar to Source Document Specialist

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  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.

ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of new medicines and treatments. As a values-driven company, ICON fosters a culture of integrity, collaboration, agility, and inclusion, employing a diverse workforce.

India

  • Provide administrative and operational support to project teams throughout the clinical research project lifecycle.
  • Coordinate meeting logistics, documentation, and stakeholder communications to ensure smooth execution.
  • Assist with data entry, report generation, and compliance with regulatory requirements.

This partner company provides clinical research project management services to clients globally. They offer a fully remote, collaborative work environment focused on quality and continuous improvement.

United States 6w PTO

  • Support operational delivery of clinical trial services including rater training, clinician network management, data management, and scale management.
  • Process clinician forms, document data, schedule training video conferences, and manage hardware shipment logistics.
  • Serve as point of contact for clinician/rater support and interact with site coordinators and CRAs for monitoring activities.

Cogstate advances brain health assessment with digital cognitive tools trusted by researchers and clinicians globally. With a global team of experts spanning psychology, data science, and operations, they have supported over 2,000 clinical trials in more than 150 countries, fostering a patient-first and collaborative culture.

US Unlimited PTO

  • Lead sponsor-side clinical data management activities across CoMind's clinical development portfolio.
  • Design, build, and configure clinical study databases including eCRF design and database validation.
  • Serve as subject matter expert on regulatory expectations and manage vendor relationships.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. The company is an early-stage startup with an AI-driven culture.

US

  • Review inpatient and outpatient medical records to ensure accurate and compliant clinical documentation.
  • Collaborate with physicians and clinical teams to clarify diagnoses and support proper coding.
  • Maintain productivity targets and contribute to provider education initiatives to improve documentation quality.

Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. It processes applications using AI to ensure fair review and shares top candidates with employers.

Hungary Poland Romania Serbia UK

  • Review, draft, and negotiate clinical trial agreements and budgets across European sites.
  • Serve as a subject matter expert and mentor to staff on contract management processes.
  • Coordinate with study teams and sponsors to ensure contract execution aligns with study timelines.

Precision for Medicine is a life sciences company that provides clinical research services. They are an established organization with a focus on supporting clinical trials and employ a global team with a culture of collaboration and professionalism.

Latin America

  • Acts as primary site contact and liaison for study management issues, ensuring compliance with ICH-GCP and regulatory requirements.
  • Manages essential document collection, maintenance, and TMF organization, and coordinates investigator recruitment activities.
  • Assists with data review, EDC entry, and supports offsite central monitoring and study supply management.

Precision Medicine Group is a clinical research organization providing services to pharmaceutical and biotech companies. The company has a global presence and fosters a collaborative culture focused on precision medicine.

US

  • Accountable for leading assigned clinical research activities and partnering with stakeholders on study design.
  • Conducts on-site and remote site visits, including qualification, initiation, monitoring, and close-out.
  • Tracks study progress, manages budgets, and mentors junior clinical study managers.

Intuitive is a pioneer and market leader in robotic-assisted surgery, dedicated to minimally invasive care. With over 25 years of experience, the company fosters an inclusive and diverse team culture where employees are empowered to do their best work.