Research Contract Analyst, Research Administration

Baptist Health

Research Contract Analyst supporting negotiation and management of clinical research contracts at Baptist Health. Collaborating with investigators and sponsors to ensure compliance with regulations.

Posted 7/28/2026full-timeRemote • Florida • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research contracts, regulatory compliance, and effective communication to facilitate contract negotiations and management. Proven ability to manage multiple contracts while ensuring adherence to federal regulations and institutional policies.

Highest-signal resume keywords

Clinical Research ContractsRegulatory ComplianceContract NegotiationExceptional Communication SkillsOrganizational Skills

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Research ProtocolsContract DraftingRegulatory RequirementsAttention to DetailLegal Issue Resolution

Soft Skills

Time ManagementWritten CommunicationVerbal Communication

Certifications & Qualifications

Certification in Clinical ResearchACRPSOCRA

Industry Keywords

FDAICH-GCPHIPAAClinical TrialsResearch Initiatives

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

The Research Contract Analyst will be responsible for supporting the negotiation, drafting, and management of contracts related to clinical research studies.
This position requires a strong understanding of clinical research protocols and regulatory requirements to ensure that agreements comply with institutional policies, sponsor/funder obligations, and federal regulations.
The Research Contracts Analyst will work closely with clinical investigators, the Office of General Counsel, and external sponsors/funders to facilitate the timely and efficient execution of contracts that support clinical trials and research initiatives.

Requirements

What you’ll need

Bachelors
Strong knowledge of clinical research contracts, regulations, and compliance requirements (FDA, ICH-GCP, HIPAA, etc.)
Certification in Clinical Research (e.g., ACRP, SOCRA) a plus, but not required.
Exceptional written and verbal communication skills, with the ability to draft clear, concise, and legally sound contract terms.
Excellent organizational and time-management skills, with the ability to manage multiple contracts and deadlines simultaneously.
Attention to detail and the ability to identify and resolve complex legal and regulatory issues.
Minimum Required Experience: 2 Years

Benefits

Comp & perks

Career growth and development opportunities, with clear pathways and ongoing support
Comprehensive health and wellness resources that go beyond traditional benefits
A wellness program that can help employees eliminate their medical plan deductible, reducing out-of-pocket healthcare costs
Tuition reimbursement to support continued learning and advancement