Clinical research assistant jobs in Compton, CA

Ability travel between site locations to conduct clinical research activities, required. 4) Prior.. ) Certified Medical Assistant, preferred. 6) Phlebotomy, EKG, and other technical skills as required..

A company is looking for a Clinical Research Coordinator (Remote). Key Responsibilities Support research physicians and maintain patient confidentiality in compliance with HIPAA standards..

The Research Coordinator will play a critical role in supporting our research projects by managing the.. Responsibilities Provide clinical research support to investigators to prepare for and execute assigned..

Clinical Research Informatician ONLY Candidates Local to the Los Angeles, CA Metropolitain area eligible.. 25k. 146k year. excellent benefits Summary. The Clinical Research Informatician is a bridge between..

Bilingual. English SpanishResponsibilities. Clinical trial management, patient communications, document.. Management of clinical trial participants, assuring..

Job Description. Clinical Research AssistantSummary. A typical Research Assistant performs a variety of.. Research queries and variances, and provide feedback to the site data collector.Input research study..

The Role Headlands Research is looking for an experienced Family Nurse Practitioner or Physician Assistant to join our team as we run cutting edge clinical research trials. The ideal candidate..

CRA I Class III West Coast Position Overview. As a Clinical Research Associate focused on medical.. Key Responsibilities. Study Management. Assist in the design and implementation of clinical study..

Job Overview. The role involves overseeing and managing clinical trials and research studies to evaluate.. Key Responsibilities. Study Management. Plan, initiate, and monitor clinical trials from start to finish..

Orders, stocks, and maintains adequate inventories of all research and office supplies. Project rollout.. Knowledge of research or medical terminology and acronyms, EHR and HIPAA policies. Exhibit..

May coordinate research project activities with other research study centers. Prepares progress reports.. May participate in the training of new team members and or clinical staff. If assigned to clinical..

If assigned to clinical trial, may work with Sponsors. monitors at clinical sites.Adheres to compliance.. ORMinimum one (1) year of experience in clinical trials protocols involving research methodology..

We are looking for a Data Entry Specialist whose main function is providing excellent customer service by quickly and accurately processing submissions sent electronically by our m..

English Spanish Responsibilities. Clinical trial management, patient communications, document.. and scheduling of meetings and appointmentsCoordinate and oversee clinical research studies from start..

This is your opportunity to start a lifelong career with unlimited opportunity. Discover the flexibility youve been searching for by taking a minute to finish our online applicatio..

JOB DUTIESDescriptionThe Clinical Research Coordinator contributes to the overall operational management.. In this role, you will be responsible for the implementation of research activities for one or more..

You will bring cutting edge research and data analysis techniques to the forefront of the ad sales.. Who You Are Education & Experience Certifications. 2 4 years of related media ad sales research..

Whether you are healthy, or have a specific illness, we'll connect you with the right trial. Potentially get paid to access the most cutting edge medicines combating your disease.

,200. 62,400 per year Location. Cupertino, CA. Onsite Role Job Summary. As a Research Moderator, you.. Requirements and Qualifications. 3 years of experience performing research studies Bachelor's degree or..