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Contracts & Consent Specialist

Insight Global

Los Angeles, CAJobSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Los Angeles, CA
Work Authorization
Not specified

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Job overview

Insight Global seeks a Clinical Research Contracts & Consent Specialist to support a leading medical device organization. The role involves managing clinical research contracts, budgeting, and informed consent activities across multiple studies, collaborating with internal stakeholders and external research sites while adapting to evolving processes and systems.

Skills & qualifications

RequiredNice to have

Skills

Clinical ResearchContracts AdministrationBudget NegotiationsInformed Consent ManagementRegulatory OperationsGood Clinical PracticeClinical Trial AgreementsMicrosoft Office SuiteCTMSeTMFContract Lifecycle ManagementStakeholder ManagementOrganizational SkillsCommunication Skills

Qualifications

2+ Years Clinical Research Experience

Full job description

Job Description

Insight Global is seeking a Clinical Research Contracts & Consent Specialist to support a leading medical device organization as it builds and expands its clinical research operations team. This individual will support clinical research contracting, budgeting, and informed consent activities across multiple studies while partnering with internal stakeholders and external research sites. The ideal candidate is highly organized, adaptable, and comfortable working in a collaborative environment where processes and systems continue to evolve.

Skills and Requirements

  • 2+ years of experience in clinical research, contracts administration, budget negotiations, informed consent management, regulatory operations, or related fields
  • Experience negotiating contracts, budgets, agreements, or working directly with external stakeholders
  • Ability to identify and escalate contractual, operational, regulatory, and compliance risks appropriately.
  • Working knowledge of Good Clinical Practice (GCP), clinical research processes, informed consent requirements, and research site operations.
  • Strong organizational skills with the ability to manage multiple priorities and deadlines simultaneously
  • Excellent written and verbal communication skills
  • Experience working in cross-functional environments with multiple stakeholders
  • Proficiency with Microsoft Office Suite
  • Experience negotiating or administering Clinical Trial Agreements (CTAs)
  • Clinical research or clinical operations experience
  • Experience supporting clinical study startup activities
  • Experience with informed consent forms (ICFs) or participant-facing study documentation
  • Knowledge of Good Clinical Practice (GCP) and clinical research regulations
  • Experience working with Institutional Review Boards (IRBs) or Ethics Committees
  • Medical device, pharmaceutical, biotech, CRO, or academic research experience
  • Experience with CTMS, eTMF, or Contract Lifecycle Management (CLM) systems Experience managing clinical trial budgets or site payment negotiations

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].

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