Jobs

Page 2: Full Time Jobs at Dm Clinical Research

(16 - 29 of 29)
  1. … Unblinded Clinical Research Coordinator II will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. DUTIES & RESPONSIBILITIES Compound and dispense presc...
    Over 4 weeks ago on The Resumator
  2. … A CRC 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 provide the best quality data to ...
    Over 4 weeks ago on The Resumator
  3. 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...
    Over 4 weeks ago on The Resumator
  4. … Unblinded CRC III will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. DUTIES & RESPONSIBILITIES Lead Unblinded team operations Compound and dispens...
    Over 4 weeks ago on The Resumator
  5. … The Senior Manager for Patient Enrollment -Therapeutics will be the driving force behind team performance, nurturing a collaborative environment, and setting the bar for exceptional customer s...
    Over 4 weeks ago on The Resumator
  6. … The Senior Manager for Patient Enrollment will be the driving force behind team performance, nurturing a collaborative environment, and setting the bar for exceptional customer service. They will spearhead ...
    Over 4 weeks ago on The Resumator
  7. … The Director of Business Development is responsible for pushing new growth in business areas and remains poised to executive growth in any channel including new trial acquisition, new therapies, new sponsor/CRO ...
    Over 4 weeks ago on The Resumator
  8. … The Site Director will ensure study enrollment to meet or exceed Sponsors' expectations, and company goals are achieved on a timely basis. The site director will also ensure that quality research is conducted at assigned investigat...
    Over 4 weeks ago on The Resumator
  9. … 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...
    Over 4 weeks ago on The Resumator
  10. … (MD/DO) The Principal Investigator will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safet...
    Over 4 weeks ago on The Resumator
  11. … The Site Director will ensure study enrollment to meet or exceed Sponsors' expectations, and company goals are achieved on a timely basis. The site director will also ensure that quality research is conducted at assigned investigat...
    Over 4 weeks ago on The Resumator
  12. … The Patient Engagement Lead will lead a growing Patient Engagement team and define, implement, and maintain reference data, business rules, and quality improvement for the organization in achieving five-star ratings in p...
    Over 4 weeks ago on The Resumator
  13. … The Patient Engagement Strategy Manager will serve as a subject matter expert in Patient Engagement, Enrollment and Retention. They will define, and implement strategic initiatives and tactics with all releva...
    Over 4 weeks ago on The Resumator
  14. … 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...
    Over 4 weeks ago on The Resumator
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