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Clinical Research Scientist – III

Role overview

Qualifications

  • PharmD with 2+ years relevant scientific and/or drug development experience
  • MS with 6+ years’ relevant scientific and/or drug development experience
  • BS or RN with 8+ years’ relevant scientific and/or drug development experience
  • Excellent verbal and written communication skills

Responsibilities

  • Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols
  • Participates in protocol review discussions concerning scientific and procedural aspects of study design
  • Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks
  • Assists in the preparation/review of regulatory documents, IND annual reports, IND safety reports, Investigator Brochures and NDAs

Key facts

Other skills

  • Presentations
  • Communication
  • Social Skills
  • Problem Solving

About the company

ICONMA logo

ICONMA

Management Consulting

We provide Professional Staffing Services & Project-Based Solutions for a broad range of Fortune 500 organizations. ICONMA is a certified Woman-Owned staffing company and was founded in 2000. ICONMA’s corporate headquarters is in Troy, Michigan, and has 15+ locations worldwide. What makes ICONMA stand out in a fiercely competitive industry? *We provide integrated, full lifecycle services across a broad range of business and technical platforms. *No single company can duplicate our full range of staffing and permanent recruiting services nationwide. *Proven track record of attracting and retaining exceedingly skilled professional workers in a highly competitive market. SERVICES OFFERED Staff Augmentation (Contract, Contract to Hire, Direct Hire, Single Source) Data Analysis Project-Based Services & Solutions Hire Train Deploy Service Model Offshore Staff Augmentation Payroll Services AREAS OF EXPERTISE - Information Technology - Engineering - Business Professional - Accounting/Finance - Admin/Clerical/Call Center - Healthcare/Clinical/Scientific - Marketing/Creative mail linkedin@iconma.com Phone (888) 451-2519 Website http://www.iconma.com

Company details

Company typeLarge
IndustryManagement Consulting
Company size1001 - 5000

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Job description

Our client, a Biopharmaceutical company, is looking for a Clinical Research Scientist - III for their Remote location.
 
Responsibilities:

  • Acquires and utilizes knowledge of clinical trial design to develop specific study concept sheets and protocols.
  • Participates in protocol review discussions concerning scientific and procedural aspects of study design.
  • Prepares study protocols, amendments, specific sections of study manuals and Investigator meeting notebooks, and other documents as needed with appropriate guidance and supervision.
  • With supervision, contributes to the design and development of CRFs, Data Management Manuals and Data Analysis Plans.
  • With supervision, addresses questions regarding scientific and related procedural issues from Investigators.
  • With supervision, contributes to the preparation and/or review of data listings, summary tables, study results, manuscripts, and scientific presentations.
  • Assists in the preparation/review of regulatory documents, IND annual reports, IND safety reports, Investigator Brochures and NDAs.
  • Supports priorities within functional area. Anticipates moderately complex obstacles within a clinical study and with guidance implements solutions.
 
Requirements:
  • PharmD with 2+ years relevant scientific and/or drug development experience
  • MS with 6+ years’ relevant scientific and/or drug development experience
  • BS or RN with 8+ years’ relevant scientific and/or drug development experience
  • May be asked to coordinate teams and provide direction.
  • May lead two or more specific components of departmental strategic initiatives.
  • Must be able to enter a new therapeutic area and summarize scientific information that is available in published literature to integrate into new study development.
  • Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies.
  • May be sought out for advice by others within the company to help make better decisions and resolve moderately complex problems.
 
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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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