Jobs

Full Time Jobs at Dm Clinical Research in Richland, Washington

(1 - 15 of 45)
  1. … - MUST BE LOCATED IN HOUSTON, TX (hybrid position) Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. The Softwa...
    6 days ago on The Resumator
  2. … The Lab Technician III 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 participating in our cli...
    1 week ago on The Resumator
  3. … The CTC II or (CRC II) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide ...
    1 week ago on The Resumator
  4. … The CTC II or (CRC II) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide ...
    1 week ago on The Resumator
  5. … The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the spon...
    2 weeks ago on The Resumator
  6. … A PBMC Laboratory Technician will be responsible for conducting special laboratory procedures for clinical trials performing high complexity laboratory techniques including, but not limited to routine isolation of peri...
    3 weeks ago on The Resumator
  7. … DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical r...
    3 weeks ago on The Resumator
  8. … The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to...
    3 weeks ago on The Resumator
  9. … The Sub-Investigator is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of subject generated data and direct...
    3 weeks ago on The Resumator
  10. … The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to...
    3 weeks ago on The Resumator
  11. Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to prov...
    3 weeks ago on The Resumator
  12. Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to prov...
    3 weeks ago on The Resumator
  13. … The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to...
    3 weeks ago on The Resumator
  14. Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to prov...
    3 weeks ago on The Resumator
  15. Clinical Research Coordinator III The Clinical Research Coordinator III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provid...
    3 weeks ago on The Resumator
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