Senior Records Information Associate

Caidya; India; Remoto; INR 600.000 - 900.000; Tempo pieno

Descrizione del lavoro

Caidya is seeking a Senior Records Information Associate to manage eTMF artifacts and support regulatory inspections. The role collaborates with global study teams to ensure TMF health, accuracy, and timely doc delivery.

The ideal candidate has ~1.5 years in records management or clinical operations, strong English communication, and meticulous attention to detail. Remote India-based position with potential cross-study work.

Competenze

• Approximately 1.5 years in records management or relevant clinical operations role.
• Healthcare or life sciences degree preferred.
• Equivalent combination of education and relevant work experience considered.

Mansioni

• Set up and maintain General, Country, and Site level artifacts within eTMFs (electronic TMFs).
• Support regulatory inspections and audits as required.
• Report document collection and tracking issues to management.
• Identify and resolve TMF document issues independently.
• Assist with study plan and core document reconciliation as needed.
• Archive study documentation and coordinate with eTMF vendor/IT.

Conoscenze

English communication

Interpersonal skills

Team player

MS Office

Attention to detail

Highly organized

Adaptable

Integrity & fairness

Formazione

Bachelor-level degree

Healthcare or life science background

Strumenti

Microsoft Office

Descrizione del lavoro

Home/Office Based Either: Home or Office Based

Job Title: Senior Records Information Associate

Job Location: India (Remote)

The Senior Records Information Associate, in collaboration with global internal and external study team members, supports all phases of the study under departmental and/or study team supervision. Duties may include Trial Master File (TMF) processing, inclusive of essential document review, such as tracking, maintaining, collecting, and coordinating content. Supports multiple studies based on scope. Has strong knowledge of the department with ability to train and mentor team members. Meets defined chargeability expectations for position.

Job Duties and Responsibilities:

• Manages the set-up and maintenance of General, Country, and Site level artifacts within electronic TMFs (eTMFs) in accordance with the Company processes and study-specific plans
• Supports regulatory inspections and/or audits as required
• Reports all document collection and tracking issues to departmental management and/or study team on a routine basis
• Proactively identifies, manages, escalates where applicable, and resolves document issues effectively and independently
• Assists with final site TMF review and close-out list creation, communicates findings, and provide feedback to applicable study team member(s)
• Assists with study plan and core document reconciliation as required
• Archives study documentation and works with eTMF vendor and IT, where applicable, to return TMF to sponsor as directed
• Prepares and provides associated reports to study teams as applicable
• Reviews, creates subfolders and maintains project mailboxes
• Conducts and documents Food and Drug Administration debarment, disqualified, and inspection lists as requested
• Files according to the Company processes and/or sponsor requirements along with the Company quality standards adhering to <95% accuracy across the major file sections and documents contained therein
• Assists in providing regular feedback to the project team on TMF health and status
• Supports conduct of departmental meetings and/or training, as applicable
• Provides support and guidance to Records Information Associates to complete assigned tasks
• Conducts other duties as assigned by departmental management (e.g., Manager, Director)

Supervisory Responsibilities:

No supervisory responsibilities.

Job Requirements:

• Education
  • College/University graduate preferred, healthcare or life science degree a plus
  • Equivalent combination of education and relevant work experience considered
• Experience
  • Approximately 1.5 years in records management or relevant clinical operations role
• Skills/Competencies
  • Strong English language written and verbal communication skills
  • Strong interpersonal skills
  • Team-oriented and a strong team player
  • Strong computer skills, including Microsoft Office
  • Exceptional attention to detail
  • Highly organized
  • Able to work in a dynamic, changing environment
  • Demonstrates honesty, trust, fairness, cooperation, self-control, and flexibility

The company will not accept unsolicited resumes from third-party vendors.