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CLINICAL DOCUMENTATION SPECIALIST

In New Jersey / United States

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CLINICAL DOCUMENTATION SPECIALIST   

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JOB TITLE:
CLINICAL DOCUMENTATION SPECIALIST
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Franklin Lakes New Jersey / United States

JOB DESCRIPTION :
Pay rate - $30/hr


The Clinical Project Leader (CPL) has the responsibility to define and implement the safety and efficacy (S&E) requirements for current and proposed products. The position is also responsible for designing and interpreting results of feasibility, clinical and human factors studies. Additionally, the CPL provides medical, scientific, and technical leadership and perspective to project teams and other functions such as Regulatory and Quality. This position is responsible for identifying, developing and /or evaluating new technologies and customer solutions in scientific disciplines within and outside of the traditional clinical laboratory. The CPL initiates and coordinates liaisons with internal/external medical, academic, regulatory and industry individuals or groups in support of business needs. The position also generates and communicates clinical and technical information to support innovation strategies, technology and product development, and product lifecycle management for marketed products. In support of all currently marketed Specimen Management (SM) products, the CPL provides technical support, associate education, troubleshooting, and competitive assessments.

PRIMARY DUTIES, RESPONSIBILITIES & AUTHORITIES:
• Represents Medical Affairs in Integrated Diagnostic Solutions (IDS) SM innovation, technology development, product development and product lifecycle management teams. Senses and defines key trends and unmet needs in science, technology, medical practice, and health economics. Reviews information and assesses risks related to vendor, material and manufacturing process changes. Provides customer and product knowledge to team. Develops safety and efficacy requirements and a clinical test plan to address S&E, Regulatory and Marketing requirements for new and improved products and gains functional approval of such. Works with the team to identify and evaluate new opportunities and present such to business leaders following the formal Innovation process. Ensures safety, efficacy and clinical utility of the product, technology, and related labelling/promotional material.
• Reviews and interprets medical/scientific data and study results, and technical literature.
Monitors trends in specimen management and other related technologies. Communicates
findings and interpretations to teams and management.
• Interacts with global medical, academic and industry experts to establish strategic direction for
innovation, technology, and product development projects.
• Provides clinical support to products entering or currently on the market including training
associates, troubleshooting, data review, interpretation and presentation, post market study
design, publications, preparation or review of regulatory communications, and addressing
quality issues.
• Designs studies, formulates and conducts scientific investigations, feasibility studies, and due
diligence studies related to new technologies and products. Interprets and presents results.
Prepares technical reports, abstracts, journal submissions and presents at scientific meetings.
• Reviews information and assesses risks related to vendor, material, and manufacturing
process changes. Designs clinical studies as needed and interprets and presents results.
• Provides medical expertise and leadership for Human Factor Engineering (HFE) studies,
Health Economics & Outcomes Research (HEOR) studies, post market surveillance and post
market studies.

KNOWLEDGE AND SKILLS:
• Knowledge of scientific methodologies and clinical laboratory medicine
• Understanding of clinical studies and study design
• Excellent interpersonal skills.
• Ability to understand, interpret and explain clinical and scientific information.
• Strong communication skills (verbal, presentation, written)

EDUCATION AND EXPERIENCE:
• BS or MS in a health-related field
• 1+ years of clinical laboratory or related healthcare field experience, or clinical research;
experience in a medical device/IVD company is a plus.
• MT(ASCP) or equivalent is desirable

Position Details

Jun 16, 2021
S16204861328189123
New Jersey / United States
Franklin Lakes
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

CLINICAL DOCUMENTATION SPECIALIST    Apply

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Pay rate - $30/hr


The Clinical Project Leader (CPL) has the responsibility to define and implement the safety and efficacy (S&E) requirements for current and proposed products. The position is also responsible for designing and interpreting results of feasibility, clinical and human factors studies. Additionally, the CPL provides medical, scientific, and technical leadership and perspective to project teams and other functions such as Regulatory and Quality. This position is responsible for identifying, developing and /or evaluating new technologies and customer solutions in scientific disciplines within and outside of the traditional clinical laboratory. The CPL initiates and coordinates liaisons with internal/external medical, academic, regulatory and industry individuals or groups in support of business needs. The position also generates and communicates clinical and technical information to support innovation strategies, technology and product development, and product lifecycle management for marketed products. In support of all currently marketed Specimen Management (SM) products, the CPL provides technical support, associate education, troubleshooting, and competitive assessments.

PRIMARY DUTIES, RESPONSIBILITIES & AUTHORITIES:
• Represents Medical Affairs in Integrated Diagnostic Solutions (IDS) SM innovation, technology development, product development and product lifecycle management teams. Senses and defines key trends and unmet needs in science, technology, medical practice, and health economics. Reviews information and assesses risks related to vendor, material and manufacturing process changes. Provides customer and product knowledge to team. Develops safety and efficacy requirements and a clinical test plan to address S&E, Regulatory and Marketing requirements for new and improved products and gains functional approval of such. Works with the team to identify and evaluate new opportunities and present such to business leaders following the formal Innovation process. Ensures safety, efficacy and clinical utility of the product, technology, and related labelling/promotional material.
• Reviews and interprets medical/scientific data and study results, and technical literature.
Monitors trends in specimen management and other related technologies. Communicates
findings and interpretations to teams and management.
• Interacts with global medical, academic and industry experts to establish strategic direction for
innovation, technology, and product development projects.
• Provides clinical support to products entering or currently on the market including training
associates, troubleshooting, data review, interpretation and presentation, post market study
design, publications, preparation or review of regulatory communications, and addressing
quality issues.
• Designs studies, formulates and conducts scientific investigations, feasibility studies, and due
diligence studies related to new technologies and products. Interprets and presents results.
Prepares technical reports, abstracts, journal submissions and presents at scientific meetings.
• Reviews information and assesses risks related to vendor, material, and manufacturing
process changes. Designs clinical studies as needed and interprets and presents results.
• Provides medical expertise and leadership for Human Factor Engineering (HFE) studies,
Health Economics & Outcomes Research (HEOR) studies, post market surveillance and post
market studies.

KNOWLEDGE AND SKILLS:
• Knowledge of scientific methodologies and clinical laboratory medicine
• Understanding of clinical studies and study design
• Excellent interpersonal skills.
• Ability to understand, interpret and explain clinical and scientific information.
• Strong communication skills (verbal, presentation, written)

EDUCATION AND EXPERIENCE:
• BS or MS in a health-related field
• 1+ years of clinical laboratory or related healthcare field experience, or clinical research;
experience in a medical device/IVD company is a plus.
• MT(ASCP) or equivalent is desirable