Clinical Research Assistant

REVA Medical, Inc.; San Diego (CA); On-site; USD 55,000 - 75,000; Full time

Job summary

REVA Medical, Inc. is seeking an administrative support specialist for Clinical Affairs in San Diego. The role centers on TMF quality controls, regulatory document management, and meeting preparations for Investigator sessions.

Ideal candidates hold an undergraduate degree with 2-3 years of clinical trial experience and familiarity with TMF processes, MS Office, and document review. This entry crosses between coordinating with sites and supporting study teams.

Qualifications

• Undergraduate degree required.
• 2-3 years of relevant clinical trial experience.
• 1-2 years of electronic Trial Master File experience.

Responsibilities

• Perform quality checks, uploads and tracking of regulatory documents to populate the electronic TMF for designated studies.
• Obtain safety-related source documents and images from clinical sites for meeting packages; coordinate with translation vendors as needed.
• Track device inventory and prepare shipments to sites, ensuring device integrity and handling of expiring items.
• Assist with distribution and tracking of study supplies to CROs and clinical centers.
• Interface with CROs to obtain study-related documentation and follow up on action items.
• Assist with site invoicing and payment tracking.
• Assist with organization and filing of study-related materials.
• Assist in the organization and execution of Investigator meetings.
• Provide general administrative support as needed.

Skills

Attention to detail

Effective communication

Document management

Regulatory knowledge

Education

Undergraduate degree

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Adobe Acrobat

Job description

Summary of Essential Duties and Responsibilities

The primary function in this position will be to provide departmental administrative support in the area of Clinical Affairs, including:

• Perform quality checks, uploads and tracking of required regulatory documents to populate the electronic Trial Master File (TMF) for designated studies. Generate reports of missing documents and upcoming expiration dates. Communicate with sites and/or study team to obtain required documents. Ensure the TMF is audit-ready in support of regulatory filings.


• Obtain safety-related source documents and images from clinical sites in preparation for Clinical Event Committee and Data Safety Monitoring Board meeting packages. Work with translation vendors as needed.


• Track device inventory and prepare shipments to sites, ensuring device integrity is maintained (i.e., temperature control and expiration dates). Process returned/expired devices.


• Assist with the distribution and tracking of clinical study supplies to Contract Research Organizations (CROs) and clinical centers (e.g. study binders, case report form worksheets, study devices and misc. materials)


• Interface with CROs to obtain study-related documentation and follow up on action items


• Assist with site invoicing and payment tracking


• Assist with organization and filing of study related materials


• Assist in the organization and execution of Investigator meetings


• Provide general administrative support as needed

Education and/or Experience

• Undergraduate degree


• 2-3 years of relevant clinical trial experience

Required Knowledge/Skills

• Minimum of 1-2 years of clinical study electronic Trial Master File experience


• Proficient with basic computer programs such as Microsoft Word, Excel PowerPoint and Adobe Acrobat


• Detail oriented in document review and error checking


• Effective communication skills

Desired Knowledge/Skills

• Minimum of 1-2 years of Sponsor or CRO experience


• Working knowledge of CDISC TMF Reference Model

Physical Demands/Working Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is frequently required to sit or stand for prolonged periods of time, frequently in front of a computer.