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DM Clinical

16 Dm Clinical Jobs Hiring Near You

DM Clinical

Clinical Research Coordinator II (3763)

Irving, TX · On-site

$23.25 - $31/hr

The Clinical Research Coordinator II (Denton, TX) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH ...

New

DM Clinical

Study Manager I (3657)

Irving, TX · On-site

$80K - $96K/yr

Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s) * Creating and or Reviewing ...

DM Clinical

Study Manager I (3612)

Melrose Park, IL · On-site

$80K - $96K/yr

Working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s) * Creating and or Reviewing ...

DM Clinical

Sub Investigator (2745)

Brookline, MA · On-site

$60 - $75/hr

Performing clinical-related procedures and/or making important trial-related decisions delegated by the Principal Investigator. * Performing clinical safety assessments and monitoring for study trial ...

New

DM Clinical

Site Manager (3510)

Brookline, MA · On-site

$100K - $120K/yr

Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA ...

DM Clinical

Site Manager (3580)

Albuquerque, NM · On-site

$100K - $120K/yr

Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA ...

DM Clinical

Site Manager (2752)

Albuquerque, NM · On-site

$100K - $120K/yr

Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA ...

DM Clinical

Lab Technician I (3611)

Houston, TX · On-site

$18.25 - $24/hr

The Lab Technician will conduct the collection of blood samples from subjects while working closely with our Clinical Research staff to provide excellent customer care to patients and their parents ...

DM Clinical

Research Assistant I (3656)

Irving, TX · On-site

$18.50 - $25.50/hr

The Research Assistant I will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIES * Completing DMCR-required training, including ...

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    Infographic showing various job openings at Dm Clinical in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.

    Unblinded Clinical Research Coordinator II (3604)

    DM Clinical

    Indianapolis, IN • On-site

    $23.25 - $30.75/hr

    Other

    Posted 28 days ago

    Job description

    DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.
    Duties & Responsibilities:
    • Compound and dispense prescribed IP as needed by Sponsor approved protocol
    • Study IP management
    • Provide training and guidance for new team members
    • Assist in all aspects of company start up activities as required
    • Supervise and maintain records of all medications
    • Ensure compliance with study-specific blinding plans
    • Perform regular audits on the clinical data to assess percent completeness and accuracy
    • Assist in onboarding training for new members
    • Ensure external sites' regulatory documents and required site certifications are up to date
    • Provide consultative support regarding the preparation and dosing of drugs
    • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction
    • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials
    • Understand and apply all applicable site procedures
    • Ensure receipt and proper storage of IP and bioretention samples, including temperature reporting
    • Develop operating procedures, guides and best practices for data entry portals and project workflows
    • Interact with Principal Investigator, sponsor, study manager and other study coordinators to ensure all aspects of protocols and study requirements are understood.
    • Any other duties or tasks assigned by the manager

    KNOWLEDGE & EXPERIENCE
    Education:
    • Associates Degree required or 2 years of formal educational coursework
    • Bachelor's degree, preferred
    • Secondary or Foreign Medical Graduate, preferred

    Experience:
    • 2+ years of Clinical Research experience, inclusive of in-clinic experience, required
    • 1+ year of Clinical Research Coordinator experience, Blinded or Unblinded, required
    • 1+ year utilizing CRIO, preferred

    Credentials:
    • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant), preferred
    • Pharmacy Technician Certification, preferred
    • Completion of DMCR-required training, including GCP, OSHA and IATA

    Knowledge and Skills:
    • Computer proficiency, especially Word, Excel, Outlook, and Google Suite products.
    • Excellent communication and customer service skills, both written and verbal
    • Excellent time-management skills
    • Ability to remain composed under pressure and high-stress situations
    • Outgoing personality
    • Well-organized with attention to detail.
    • Must be able to multitask.
    • Bilingual (Spanish) preferred

    Apply