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Clinical Research Specialist

Motion Recruitment Partners, LLC

Remote or Irvine, California • Today

Easy Apply

Contract

Clinical Research Scientist III - (Director/Assoc. Director level)

NexInfo Solutions, Inc.

Remote or Hybrid in Parsippany-Troy Hills, New Jersey • 10d ago

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Third Party, Contract

$100 - $110

Clinical Research Leader

Motion Recruitment Partners, LLC

Remote or New Brunswick, New Jersey • Today

Easy Apply

Contract

Motion Recruitment Partners, LLC

Job Details

Skills

Research and Development
Standard Operating Procedure
Accountability
Interfaces
Payments
Statistics
Publications
Data Collection
Budget
Management
Policies and Procedures
Supervision
Decision-making
Life Sciences
Nursing
Biology
RAC
Google Cloud Platform
Google Cloud
ISO 9000
Medical Devices
Clinical Research
Science
Clinical Trials
Research
Regulatory Compliance
Presentations
Technical Writing
English
Communication

Summary

Kelly Science and Clinical FSP is currently seeking a Clinical Research Specialist for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This position is hybrid. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.

SECTION 1: JOB SUMMARY
This Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.
SECTION 2: DUTIES & RESPONSIBILITIES
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate, procedures and guidelines, this position:

Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, under supervision
Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-Google Cloud Platform, applicable legislation and Company Standard Operating Procedures
May serve as the primary contact for clinical trial sites (e.g. site management)
Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports)
Supports applicable trial registration (e.g. from study initiation through posting of results and support publications as needed
Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials
Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel
Interfaces and collaborates with Clinical Research Associates (CRAs)
Assists in overseeing and supports the development and execution of Investigator agreements and trial payments
Assists in clinical data review to prepare data for statistical analyses and publications
May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need
May provide on-site procedural protocol compliance and data collection support to the clinical trial sites
Assists in tracking assigned project budgets
May perform other duties assigned as needed
Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures
Should develop a strong understanding of the pipeline, product portfolio and business needs
Generally manages work with supervision. Independent decision-making for simple situations but requires guidance for complex situations.

SECTION 3: EXPERIENCE AND EDUCATION
Education

Minimum of a Bachelor's Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

Experience

BS with at least 2 years, MS and PhD with at least 1 year of relevant experience preferred.
Previous experience in clinical research or equivalent is desired.
Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, Google Cloud Platform, ISO 14155, MDR, MEDDEV,...).
Clinical/medical background is a plus.
Medical device experience is a plus.

SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS
Functional and Technical Competencies:

Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations
Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations
Presentation and technical writing skills
Written and oral English communication skills.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 10105282
Position Id: 885041
Posted 10 days ago

Company Info

About Motion Recruitment Partners, LLC

Motion Recruitment delivers IT Talent Solutions for Contract, Direct Hire, Managed Solutions and Statement of Work to all of North America from our 21 delivery centers. Our high-touch, specialized, team-based recruitment model’s success is proven through our exemplary track record in filling the most challenging IT positions for startup and enterprise clients alike. Our hyper-specialized tech focus results in a truly consultative approach for both our clients and candidates, within our recruiting areas of expertise: Software, Mobile, Data, Infrastructure, Cybersecurity, Product + UX and Functional.

Motion also delivers IT Consulting Solutions through the Motion Consulting Group (MCG) that create true digital transformation for IT projects in Agile Development & Coaching, DevOps & DevSecOps Solutions, and Managed Services for IT Operations.

We’re also the proud creators of Tech in Motion and the Timmy Awards, our North American community platform, events series and award program that connects over 250,000 tech enthusiasts to meet, learn, and innovate.

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Motion Recruitment Partners, LLC

Job Details

Skills

Research and Development
Standard Operating Procedure
Accountability
Interfaces
Payments
Statistics
Publications
Data Collection
Budget
Management
Policies and Procedures
Supervision
Decision-making
Life Sciences
Nursing
Biology
RAC
Google Cloud Platform
Google Cloud
ISO 9000
Medical Devices
Clinical Research
Science
Clinical Trials
Research
Regulatory Compliance
Presentations
Technical Writing
English
Communication

Summary

Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, under supervision
Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-Google Cloud Platform, applicable legislation and Company Standard Operating Procedures
May serve as the primary contact for clinical trial sites (e.g. site management)
Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports)
Supports applicable trial registration (e.g. from study initiation through posting of results and support publications as needed
Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials
Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel
Interfaces and collaborates with Clinical Research Associates (CRAs)
Assists in overseeing and supports the development and execution of Investigator agreements and trial payments
Assists in clinical data review to prepare data for statistical analyses and publications
May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need
May provide on-site procedural protocol compliance and data collection support to the clinical trial sites
Assists in tracking assigned project budgets
May perform other duties assigned as needed
Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures
Should develop a strong understanding of the pipeline, product portfolio and business needs
Generally manages work with supervision. Independent decision-making for simple situations but requires guidance for complex situations.

SECTION 3: EXPERIENCE AND EDUCATION
Education

Minimum of a Bachelor's Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

Experience

BS with at least 2 years, MS and PhD with at least 1 year of relevant experience preferred.
Previous experience in clinical research or equivalent is desired.
Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, Google Cloud Platform, ISO 14155, MDR, MEDDEV,...).
Clinical/medical background is a plus.
Medical device experience is a plus.

SECTION 4: REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS
Functional and Technical Competencies:

Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations
Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations
Presentation and technical writing skills
Written and oral English communication skills.

Dice Id: 10105282
Position Id: 885041
Posted 10 days ago

Company Info

About Motion Recruitment Partners, LLC

Go to company profile

Fitment

Dice Job Match Score™

🔢 Crunching numbers...

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