Clinical Research Assistant Job

CLINICAL RESEARCH ASSISTANT needed for a CONTRACT opportunity with Yoh's client located in San Francisco, CA.

TOP SKILLS SHOULD YOU POSSESS:

- Data Entry
- TMF duties

WHAT YOU'LL BE DOING:

- Completes tasks in creative and effective ways.
- Works on assignments requiring considerable judgment and initiative.
- Understands implications of work and makes recommendations for solutions.
- Determines methods and procedures on new assignments.
- Provides support to clinical research including, but not limited to, maintenance of documentation, clinical tracking and information retrieval.
- Performs general administrative functions such as, scheduling meetings and requesting proposals/contracts from TMF/eTMF Vendors, tracking and helps to ensure payments are on time.
- Performs data entry into designated clinical tracking systems in accordance with project requirements, including collection of information from designated clinical team members, CROs, vendors, etc.
- Serves as key central contact for communications, correspondence and associated documentation.
- Performs TMF duties such as, paper and electronic filing of clinical study records consisting of correspondence, lab reports, drug shipments, enrollment, safety letters, Clinical Monitoring Reports, and other study documents.
- Also, responsible for document retrieval as requested by clinical teams.
- Maintains and ensures all TMF/eTMF documentation are in a state of audit-readiness.
- Responsible for collection, dissemination, and/or tracking of financial disclosure documents as required.
- Performs all responsibilities in accordance with Standard Operating Procedures, established guidelines and work instructions, and appropriate industry and Good Clinical Practices standards.
- Assists in the coordination of documentation associated with conducting clinical studies for the TMF and eTMF.
- Assists CRAs and other clinical staff in the management of documentation required for clinical studies conduct.
- Supports the creation of standardized clinical trial TMF: tools, processes and trackers.
- Responsible for exporting the metrics surrounding clinical studies TMF document tracking and data entry.
- Supports other projects as assigned.

WHAT YOU NEED TO BRING TO THE TABLE:

- Requires a minimum of a High School diploma.
- Equivalent experience may be accepted.
- A minimum of four (4) years industry experience working in the Pharmaceutical, Biotechnology or other related industry is required.
- Strong attention to detail is a must.
- Good communication skills both oral and written are a must.
- Good computer skills are required.
- Working knowledge of MS Word, Excel, and

PowerPoint is required.
- Excellent organizational skills are required.
- Must have an ability to multi-task.

BONUS POINTS! OTHERWISE KNOWN AS PREFERRED QUALIFICATIONS:

- An Associates degree is a plus.

WHAT ARE YOU WAITING FOR? APPLY NOW!

RECRUITER: Will Thompson

Yoh, a DayTHIS ADDRESS IS EXCLUSIVELY FOR INDIVIDUALS WITH DISABILITIES REQUESTING APPLICATION ASSISTANCE.

J2W: SCIENTIFIC

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SFSF: LS