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Kelly Services Clinical Research Coordinator- Pulmonary and Cardio Trials in Palm Springs, California

Groundbreaking, academic trained, and ethical start-up clinical research group looking for an ambitious and talented Clinical Research Coordinator who can excel under relative autonomy and is willing to commit the time and effort to learn and grow with the company.

Candidate must be comfortable with accounting and budgeting of procedures to invoice sponsor using CTMS, and must be able to work onsite or remotely remotely. Ability and receptiveness to undertaking a variety of patients and indications is a must. As trials grow and are successful, compensation bonuses are promised and fulfilled.

Schedule is variable and will include at home work days.

Clinical Research Coordinator Job Description

Although the PI is responsible for the conduct of the trial, it has been said that the CRC is the heart and soul of the research study and that, ultimately, it is the CRC who carries forward the research goals, thereby playing a significant role in the success of the research study.

Responsibilities

  • Primary responsibility is the ability to inputting schedule of events of all trials the company conducts into CTMS and keeping track of events and invoiceable procedures.

  • Ability to jump in and Conduct clinical trials using good clinical practice GCP under the auspices of a Principal Investigator PI .

  • Good clinical practices principles include but are not limited to the following activities: Trials are conducted ethically, as defined by the Declaration of Helsinki, rigorously, as defined by the International Conference on Harmonization Guidelines ICH .

  • Benefits outweigh risks for each patient. Rights, safety and well-being of patients prevail over science. All available nonclinical and clinical information on any investigational agent can support the trial as designed.

  • All trials are scientifically sound and clearly described. All clinical trials have current Institutional Review Board approval. Medical decisions and care are the responsibility of qualified health care professionals, specifically physicians and, if applicable, dentists.

  • Everyone involved in the clinical trial is qualified by training, education and experience. Informed consent is given freely by every participant. All study documentation is recorded, handled and stored to allow accurate reporting, interpretation and verification.

  • Confidentiality of subjects is respected and protected. Investigational products maintain Good Manufacturing Practice in storage, manufacturing and handling. Systems to ensure quality are implemented in all aspects of the trial.

Duties and Tasks

  • Interact with all CRCs and assistants in all locations to understand current protocols and add events contemporaneously into CTMS.

  • Keep track of payments sent by sponsor and reconcile them with any invoiceable procedures that were not included may be called upon to take own trial and thus Code, evaluate, or interpret collected study data.

  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional policies.

  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.

  • Communicate with laboratories or investigators regarding laboratory findings. Order drugs or devices necessary for study completion.

  • Direct the requisition, collection, labeling, storage, or shipment of specimens.

  • Arrange for research study sites and determine staff or equipment availability.

  • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.

Why Kelly ® ?

Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

About Kelly ®

At Kelly, we’re always thinking about what’s next and advising job seekers on new ways of working to reach their full potential. In fact, we’re a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law. (https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm)

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