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Clinical Research Leader

Motion Recruitment Partners, LLC

Remote or New Brunswick, New Jersey • Today

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Contract

Senior Manager, Clinical Programming

Genmab

Princeton, New Jersey • Today

Full-time

USD 131,040.00 - 196,560.00 per year

Senior Clinical Research Specialist

Motion Recruitment Partners, LLC

Remote or Irvine, California • Today

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Contract

Clinical Quality Project Manager

Della Infotech

Remote • Yesterday

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$60 - $78

Clinical Trial and Data Support Consultant

NexInfo Solutions, Inc.

Remote • 3d ago

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Third Party, Contract

$50 - $60

Clinical Data Enablement Senior Manager

Siro Clinpharm Pvt Ltd

Remote or Hybrid in Mexico Beach, Florida • 13d ago

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Full-time

Depends on Experience

Senior User Researcher

Office of Technology and Innovation

New York, New York • Today

Full-time

Head of Clinical Data Management

Insmed Incorporated

Remote or New Jersey • Today

Full-time

USD 255,000.00 - 347,500.00 per year

Principal Clinical Trial Coordinator - FSP

Thermo Fisher Scientific

Remote • Today

Full-time

Artificial Intelligence Research Lead - Vice President

JPMorgan Chase & Co.

New York, New York • Today

Full-time

USD 164,350.00 - 260,000.00 per year

Director, Chemical Engineering R&D

Merck & Company Inc

Rahway, New Jersey • Today

Full-time

USD 173,200.00 - 272,600.00 per year

AI Technical Lead

University of Wisconsin-Madison

Remote or Madison, Wisconsin • Today

Full-time

USD 115,000.00 - 140,000.00 per year

Director - Pharmacometrics AI Lead (Remote or Hybrid)

Merck & Company Inc

Remote or Rahway, New Jersey • Today

Full-time

USD 190,800.00 - 300,300.00 per year

AI Practice Lead - Life Sciences & Healthcare

EPAM Systems

Remote or New York, New York • Today

Full-time

Lead Healthcare Product Owner

System One

Remote • 13d ago

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Contract

$72.18

Engineering and Technology Leader

GE Vernova

Parsippany-Troy Hills, New Jersey • Today

Full-time

USD 172,800.00 - 288,000.00 per year

AI Practice Lead - Life Sciences & Healthcare

EPAM Systems

Remote • Today

Full-time

Medical Director

CitiusTech

Remote • 3d ago

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Contract

180 - 200

Lead – Product Research

Business Software, Inc.

Remote • 9d ago

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Full-time

120000 - 135000

Medical Director

Tekcel8

Remote • 3d ago

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Contract

Depends on Experience

AI Research Lead (Natural Language Processing) - Vice President

JPMorgan Chase & Co.

New York, New York • Today

Full-time

USD 164,350.00 - 260,000.00 per year

Sr. Clinical Scientist

Motion Recruitment Partners, LLC

Remote or Rahway, New Jersey • Today

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Contract

Motion Recruitment Partners, LLC

Job Details

Skills

Research and Development
Standard Operating Procedure
Accountability
Payments
Statistics
Publications
EDS
Data Collection
Collaboration
Partnership
Team Leadership
Business Plans
Messaging
Policies and Procedures
Supervision
Decision-making
Life Sciences
Nursing
Biology
RAC
Google Cloud
Google Cloud Platform
ISO 9000
Medical Devices
Science
Dynamics
Health Care
Clinical Trials
Clinical Research
Product Development
Management
LCM
Research
Budget
Regulatory Compliance
Presentations
Technical Writing

Research and Development
Standard Operating Procedure
Accountability
Payments
Statistics
Publications
EDS
Data Collection
Collaboration
Partnership
Team Leadership
Business Plans
Messaging
Policies and Procedures
Supervision
Decision-making
Life Sciences
Nursing
Biology
RAC
Google Cloud
Google Cloud Platform
ISO 9000
Medical Devices
Science
Dynamics
Health Care
Clinical Trials
Clinical Research
Product Development
Management
LCM
Research
Budget
Regulatory Compliance
Presentations
Technical Writing

Summary

Clinical Research Leader
Summary:
This Clinical Research Leader will be responsible for leading and supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.
Responsibilities:

Serve as a Clinical Research Leader within the Clinical R&D Department to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones
Oversight/execution of 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)
Develop clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports) with minimal supervision
Ensure applicable trial registration from study initiation through posting of results and support publications as needed; (e.g. on
Management/oversight of ordering, tracking, and accountability of investigational products and trial materials
Interface and collaborate with site personnel, IRBs/ECs, contractors/vendors, and company personnel
Oversee the development and execution of Investigator agreements and trial payments
Responsible for clinical data review to prepare data for statistical analyses and publications
If applicable, may perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need
May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects
If applicable, as part of a clinical trial, may provide on-site procedural protocol compliance and data collection support to the center
Contribute to the critical assessment of the literature and to the interpretations and disseminations of all evidence generated
Responsible for delivery of assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs)
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
Track and manage assigned project budgets to ensure adherence to business plans
Support clinical scientific discussions with regulatory agencies/ notified bodies to drive support of the clinical and regulatory strategy
Develop a strong understanding of the pipeline, product portfolio and business needs
May serve as the clinical representative on a New Product Development team
May be responsible for development of Post-Market Clinical Follow-up (PMCF) Plans and Reports
May conduct review of promotional materials to ensure fair-balance, accuracy in clinical claims and messaging
Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures
Manage resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency
Perform other duties assigned as needed
Generally manages work with limited supervision, dependent on project complexity Independent decision-making for simple and more advanced situations but require minimal guidance for complex situations

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

Previous experience in clinical research or equivalent is required
Experience working well with cross-functional teams is required
Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, Google Cloud Platform, ISO 14155, MDR, MEDDEV)
Clinical/medical background a plus
Experience managing projects a plus
Medical device experience highly preferred

Functional and Technical Competencies:

Good understanding of clinical research science and processes along with an understanding of product development processes, team dynamics, related healthcare market environment, clinical trends, and global clinical trial regulations
Ability to provide scientifically strategic and scientific clinical research input across New Product Development (NPD) and Life-Cycle Management (LCM) projects
Proven track record in delivering clinical projects within clinical/ surgical research setting, on time, within budget and in compliance to SOPs and regulations
Strong presentation and technical writing 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: 876135
Posted 30+ 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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Position Summary The Clinical Data Coordinator is responsible for supporting the collection, review, reconciliation, and maintenance of high-quality clinical trial data across studies managed by the organization. This position works closely with Clinical Research Coordinators, Investigators, Clinical Research Associates, Project Managers, sponsors, CROs, and other study team members to ensure clinical data are complete, accurate, timely, and compliant with study protocols, Good Clinical Practic

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Remote or Irvine, California

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Sr. Clinical Scientist

Remote or Rahway, New Jersey

•

Today

Sr. Clinical Scientist Kelly Science and Clinical FSP is currently seeking a Sr. Clinical Scientist for a long-term engagement with one of our Global Pharmaceutical clients. 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 will be eligible for Medical, Dental, Vison, 401K, and a variety of other benefits to choo

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