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Contractual Contract Clinical Research Jobs (NOW HIRING)

GDIT

Sr. Clinical Research Director (TBI)

Tacoma, WA · On-site

Assists other contract service providers, military commanders and community agencies in the ... Rather, salary will be set based on experience, geographic location and possibly contractual ...

NYULMC

Program Lead, Clinical Research

New York, NY · On-site

Collaborates with investigators, departmental leadership, OSR units, contracts, sponsored programs ... contractual, operational, financial, and regulatory timelines. * Oversees development and ...

Deaconess

Research Contracts Admin

Evansville, IN · On-site

$19.14 - $26.79/hr

... clinical trial agreements, budgets, amendments, and contract extensions * Serve as a liaison between research teams, sponsors, CROs, and financial stakeholders * Monitor compliance with contractual ...

Teleflex

Clinical Contracts Analyst (REMOTE)

Boston, MA · Remote

$75K - $90K/yr

Clinical contract work experience from pharmaceutical, medical device, healthcare, or Contract Research Organizations (preferred). Experience with contractual agreements, including master services ...

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Contractual Contract Clinical Research information

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How much do contractual contract clinical research jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for contractual contract clinical research in the United States is $27.65, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $29.81 per hour, depending on experience, location, and employer.

What is the difference between Contractual Contract Clinical Research vs Contractual Clinical Research Coordinator?

AspectContractual Contract Clinical ResearchContractual Clinical Research Coordinator
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonRequires similar credentials; often holds a degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentConducts clinical trials, manages study protocols, and liaises with sponsors in research settingsCoordinates daily clinical trial activities, enrolls patients, and ensures protocol adherence at research sites
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for contractual research rolesCommonly employed by hospitals, research centers, and clinical trial sites

Both roles involve clinical research but differ mainly in scope and responsibilities. Contractual Contract Clinical Research professionals often oversee entire studies or projects, while Contractual Clinical Research Coordinators focus on day-to-day trial coordination at research sites. Understanding these differences helps in choosing the right career path or job opportunity.

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Contractual Contract Clinical Research jobs near you
Infographic showing various Contractual Contract Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $57,519 per year, or $27.7 per hour.

Clinical Research Contract Specialist (Full Time, Days)

Nicklaus Children's Health System

Miami, FL • On-site

Contractor

Posted 11 days ago

Job description

Description
Job Summary: Facilitates preparation and execution of contractual agreements with pharmaceutical, biotechnology, medical device and technology companies, academic institutions, and physician practices. Coordinates efforts to help ensure Research Institute, suppliers, and customers have contractual agreements in place that are clear, fair and legally binding. Oversees and coordinates day to day administrative functions associated with the contracting process within organization's Human Research Protections Program (HRPP) at the Research Institute and the Office of Sponsored Programs (OSP). Minimum Job Requirements: Bachelor's Degree Business Administration, or other relevant field required (Required) 2-4 years experience incontract negotiation
Qualifications
Knowledge, Skills and Abilities Juris Doctorate or Master's degree in relevant field preferred Prior experience in clinical trials contract negotiation highly preferred 3 years of research experience preferred Experience in pediatric clinical research in a hospital setting preferred Clinical research certification (such as ACRP, MAGI or SOCRA) preferred Experienced with electronic medical record and clinical trial management software applications preferred Working knowledge of Federal, State and/or International research regulations Excellent communication and relationship building skills Detail-oriented with excellent organizational skills Self-confident, flexible, and adaptable to change Demonstrated ability to manage multiple complex projects simultaneously Proficient with basic software applications including Word, Excel, and PowerPoint ESSENTIAL JOB DUTIES: Ensures clinical research and related activities are performed in accordance with all applicable Federal regulations, Research Institute, NCHS and sponsor policies and procedures. Creates, drafts, and reviews contractual agreements and grant award documents. Performs initial and ongoing review and provides comments on contractual agreements received from clients and suppliers including AAHRPP language. Prepares contract approval timelines with all parties involved and leads follow-up efforts to obtain contract approval. Ensures contracts are accurate, complete, signed by the appropriate parties and submitted in a timely manner. Conducts contract negotiations and participates in client interactions. Engages with Nicklaus Children's Health System's General Counsel as needed to review contract terms and assist with developing research-appropriate contract templates. Ensures consistency of terms between informed consent forms and agreements. Manages dissemination and filing of contractual agreements through email and contract tracking database. Coordinates efforts, as directed, among Research Institute clients (internal and external), suppliers and vendors to facilitate timely execution of agreements Maintains up-to-date tracking of all contracts and client correspondence to provide periodic internal updates. Prepares ad hoc reports. Uses standard computer applications as well as legal/contract software to standardize and improve departmental processes and tracking. Reviews, negotiates, and processes vendor agreements and correspondence as requested by Research Institute and OSP leadership. Creates and manages study profiles within the Clinical Trial Management System (CTMS). Assigns internal financial tracking number to each study and communicates with Finance in order to activate the number in Nicklaus Children's Health System's financial system.

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