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Biotechnology Research

Source Document Specialist

United StatesOnsiteFull TimeEntry-level (exp-based)Posted 1 month ago

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Required skills

  • Source Documents
  • Version Control
  • Study Teams
  • Vendors
  • Sponsors
  • Study Coordinators
  • Investigators
  • GCP
  • FDA
  • Audit Preparation

Nice to have

  • Medical Experience
  • Team Lead
  • Office Equipment
  • Team Mentality
  • Task Management
  • Prioritization

Role summary

The Source Document Specialist is responsible for creating and maintaining study source documents for clinical research studies, ensuring compliance with GCP, FDA, and sponsor requirements. This role involves version control, acting as a liaison between study teams, vendors, and sponsors, and providing training on best practices. The specialist will also assist with audit preparation, maintain data security, and identify process improvements to enhance departmental efficiency. A minimum of 6 months of medical experience is preferred, along with strong attention to detail, communication, and task management skills.

The role of the Source Document Specialist is responsible for creating and maintaining study source documents throughout assigned studies.

 To consistently embody AMR Clinical’s Core Values:

  • United We Achieve
  • Celebrate Diverse Perspectives
  • Do the Right Thing
  • Adapt and Persevere

The Source Document Specialist reports to the Source Document Team Lead.

Classification: Non-Exempt

Primary Responsibilities: 

  • Maintain version control and tracking of all study source documents.
  • Serve as a liaison between study teams, vendors, and sponsors to ensure document accuracy and completeness.
  • Communicate with study coordinators and investigators to clarify documentation requirements.
  • Provide training and guidance to team members on best practices for source documentation.
  • Identify opportunities to streamline source document workflows for improved efficiency.
  • Ensure source documents comply with Good Clinical Practice (GCP), FDA, and sponsor requirements.
  • Assist with audit preparation by ensuring all source documents are complete and readily accessible.
  • Maintain confidentiality and data security in handling sensitive study-related information.
  • Create study source documents, utilizing the study protocol, lab manual, pharmacy manual and EDC guidelines for each study. 
  • Review and approve created study documents for each study. Ensuring accuracy and all components of the study are captured.
  • Maintain and evolve efficiencies within the department
  • Position may require occasional weekend and/or overtime hours. 
  • Other duties as assigned

Desired Skills and Qualifications:

  • At least 6 months of medical experience.
  • Ability to effectively lead a high-performance team
  • Devote keen and acute attention to detail
  • Ability to operate basic office equipment including but not limited to copy machines, facsimile machines and computers. 
  • Strong verbal and written communication skills
  • Strong interpersonal skills
  • Positive, collaborative, team mentality
  • Excellent task management and prioritization skills
  • Build and cultivate long term relationships
  • Excellent follow up
  • Drive and initiative 
  • Fluent in English.

AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.

** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.

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