Clinical Data Analyst III

Integrated Resources Inc.; City of Rochester (NY); On-site; USD 80,000 - 110,000; Full time

Job summary

A prominent staffing firm seeks a Clinical Data Analyst III for a 1-year project. This role involves assessing product classifications and technical documentation gaps within the regulated healthcare space, as well as creating performance evaluation reports and liaising with project leads. Ideal candidates will have over 5 years of relevant experience, particularly in R&D or Clinical Affairs, and demonstrate strong analytical and problem-solving skills within the medical device industry.

Qualifications

• 5+ years’ experience in regulated healthcare industry, preferably in Medical Device/IVD.
• Experience in R&D or Clinical Affairs role preferred.
• Experience in technical and clinical data review.

Responsibilities

• Assess technical documentation for Ortho products and identify gaps.
• Create draft Performance Evaluation reports.
• Propose opportunities for addressing gaps with external data sources.

Skills

Attention to detail

Problem-solving

Excellent verbal skills

Excellent written skills

Presentation skills

Tools

Microsoft Office Suite

Adobe

SharePoint

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Title: Clinical Data Analyst III

Duration: 1 year

Responsibilities:

• The Responsibilities: Based on the classification assessment of the Ortho products undertake an assessment of a sample of different classes of product against the Technical Documentation (Annex II - 2017/746) and identify any gaps and in particular significant gaps.
• From the representative product sample identify the time and resources required to address any gaps that can be used for budget planning purposes in 2018/19, particularly if product testing or performance evaluations are required.
• Create draft Performance Evaluation reports for a representative sample of Class B, C and D products.
• Propose opportunities for filling any identified gaps with data from other sources such as published literature, post-market data.
• Provide periodic updates to the IVDr Project Lead at a frequency to be determined.

Qualifications

Qualifications:

Experience:

• 5+ years’ experience in a role in regulated healthcare industry and preferably in a Medical Device/IVD regulated industry
• Preferable experience having worked in an R&D or Clinical Affairs role.
• Experience in technical and clinical data review.
• Attention to detail and problem-solving.
• Excellent verbal, written and presentation skills.
• Ability to work independently

Desired Competencies:

• Working knowledge of EU IVD regulations
• Working knowledge of IVD products and regulations
• Familiarity with web-based content sharing applications (i.e. SharePoint), Microsoft Office Suite, Adobe.

Additional Information

Kind Regards,

Clinical Recruiter

Integrated Resources, Inc.

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