Clinical Data Coordinator-3722

Description

One of our clients is seeking a talented and highly motivated Sr Clinical Operations Representative. Please send your resume if you would like to pursue this opportunity and authorize Infosoft to represent you for this position.

Here are the job position details for your review:

Job Title: Sr Clinical Operations Representative
Pay Rate: $29 to 31/Hr
Duration: 18 Months
Location: Remote (8 AM to 5 PM Pacific Time)

Our Client is a Global Medical Device Manufacturer.

We are looking for a Sr. Clinical Operations Representative with responsibility for the efficient processing and quality check of all clinical study documents.

The main function of a clinical operations representative is to be responsible for efficient processing and quality checks of all study documents.

• Conduct periodic audits of documentation and may participate in internal master file audits
• Review and ensure accuracy and completeness of clinical study files and/or device accountability logs, enter into a computerized tracking system, and file/scan for archive, for multiple clinical research trials
• May be required to work in the coordinator role as dictated by business needs
• Monitor device inventory by coordinating with Supply Chain and Clinical Specialists
• Other incidental duties (e.g. occasional photocopying or deliveries)

Top Skills:

• High level of detail-oriented, lots of data entry and templates
• High level of communication
• Transcribe notes, medical terminologies

Additional Skills:

• Good computer skills including MS Office Suite, Adobe, and ability to operate general office machinery
• Experience with ERP software, JDE, and CTMS (Clinical Trial Management System) preferred
• Good written and verbal communication skills and interpersonal relationship skills
• Ability to work in a fast-paced environment
• Substantial knowledge and understanding of clients' policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical study documentation
• Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint
• Good problem-solving skills
• Ability to manage confidential information with discretion
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Must be able to work in a team environment under minimal supervision
• No instructions are needed on routine work, and general instructions are given only on new lines of work or special assignments
• Adhere to all EHS rules and requirements and take adequate control measures in preventing injuries to themselves and others as well as to the protection of the environment and prevention of pollution under their span of influence/control

Education and Experience:

• H.S. Diploma or equivalent
• 5-7 years of experience

Job Types: Contract, Full-time

Salary: $29.00 - $31.00 per hour

Schedule:

• 8 hour shift

Application Question(s):

• please provide your email address

Education:

• High school or equivalent (Required)

Experience:

• clinical trail documentation: 2 years (Required)
• Medidata , TMF: 1 year (Required)
• Transcribe notes: 1 year (Required)

Work Location: Remote