Clinical Research Coordinator -244778 Job at Medix™, Modesto, CA

N0l0NlFLK1VWS0VEeFBzVTI4NHhqaXFNY2c9PQ==
  • Medix™
  • Modesto, CA

Job Description

**Seeking a Clinical Research Coordinator in Modesto, CA**

Come and join our team! We are a local growing private medical practice specializing in the diagnosis and treatment of patients with diseases of the retina and vitreous. We are looking for individuals who would like to establish a career in healthcare working with nationally recognized physicians. We provide on the job training giving you the ability to grow and advance your skills along with gaining innovative knowledge. Established in 1977, we have locations all over Northern California including Sacramento, Grass Valley, Roseville, Stockton, Modesto, Merced, Fairfield, Elk Grove, Folsom, Yuba City and Chico. Our physicians are nationally known, and we continue to be on the leading edge of retina care by utilizing the latest equipment and both participating in and designing new clinical trials to advance the state of care for retinal diseases. Join 250+ other team members working for our nationally recognized retina specialty practice in a fast paced, high volume medical office.

The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

We seek a full-time clinical research coordinator to support our clinical research department. Although you must be able to work independently, you will be working directly with physicians, patients, research coordinators, clinical and business office staff and with pharmaceutical sponsor representatives to correctly and efficiently execute clinical research protocols. Collaboration and being a team player are essential to the success of this role.

As our clinical research coordinator, you will assist in the planning, development and implementation of clinical research trials involving the study of agents to treat diseases of the retina, macula and vitreous.

Responsibilities:

  • Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
  • Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand
  • Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals, etc.) and that the training is documented
  • Creates, manages, and maintains source documents for each trial
  • Attends teleconferences and Investigator Meetings as requested by research director
  • Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections
  • Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals
  • Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately
  • Efficiently completes all study tasks delegated to them (i.e. scribing, VFQ, IOP, etc.)
  • Conducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the study
  • Assures that amended consent forms are appropriately implemented and signed
  • Acts as a secondary reviewer to provide oversight so that the ICF process is conducted accurately
  • Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract.
  • Oversees data and ensures that it is being entered correctly and resolves any queries issued within required timeframe
  • Collects and reports ALL Adverse Events
  • Collects and reports ALL Serious Adverse Events
  • Responsible for ensuring all SUSAR/Safety Reports are acknowledged and reviewed
  • Coordinates monitor site visits and assists with preparation of site visit documentation
  • Works with the monitor to make any corrections needed to meet requirements and deadlines as needed
  • Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required timeframe
  • Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, Investigator disclosures, CVs, training documentation, instructions on reporting requirements for the IRB and the sponsor.

Job Tags

Full time, Contract work, Private practice, Work at office, Local area,

Similar Jobs

Hyatt

Spa Therapist Job at Hyatt

 ...You will be responsible to provide an excellent and consistent level of service to your customers. The Spa Therapist is responsible to perform professional massage therapy, body treatments, facials, manicures, pedicures and waxing (aesthetic services) and remain current... 

Arkansas Staffing

Agricultural Equipment Operator Job at Arkansas Staffing

 ...Seasonal/Temporary Agricultural Equipment Operator Worker will be required to perform a variety of duties such as: mix specified materials...  ...harvesting, storing crops; operate or tend large, high horsepower farm equipment used in agricultural production such as tractor,... 

CFO's Domain

Fractional CFO (San Francisco) Job at CFO's Domain

 ...This range is provided by CFO's Domain. Your actual pay will be based on your skills and experience talk with your recruiter to learn...  ...organizational transitionwithout operating as a day-to-day full time Controller. QUALIFICATIONS ~ Bachelors degree in Accounting,... 

Optum

RN Private Duty - Sparta Job at Optum

 ...incentives. The hourly pay for this role will range from $28.27 to $50.48 per hour based on full-time employment. We comply with all minimum wage laws as applicable. #LHCJobs At UnitedHealth Group, our mission is to help people live healthier lives and make the health... 

Pro Standard

Social Media Manager Job at Pro Standard

 ...Content Strategy + Planning Own and lead the development of social content calendars across Pro Standard and future client brands...  ...and social amplification Qualifications ~35 years of social media experience in-house or agency-side, ideally with lifestyle, fashion...