clinical trial educator - Deerfield, United States - Randstad

    Default job background
    Description
    clinical trial educator.

    deerfield , illinois (remote)

    posted 7 days ago

    job details

    summary

    $55 - $60.83 per hour

    contract

    bachelor degree

    category life, physical, and social science occupations

    reference48002

    job details


    job summary:


    As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena.

    Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions.

    A longtime partner who prides itself on being a leader in many different practical manufacturing processes to better serve the entire population is renowned for pioneering new treatments for renal diseases, immune disorders, and more; the focus is on patient care.

    If you're looking to be a part of an impactful team, you won't be disappointed


    This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.


    location:
    Deerfield, Illinois


    job type:
    Contract


    salary:
    $ per hour

    work hours: 9 to 5


    education:
    Bachelors


    responsibilities:
    CTE analysis of data for optimal site selection

    Expedited contracts and documentation completion

    Responsible to facilitate trainings, vendor readiness, system access, study supplies, IP, patient waitlist review and prescreen database

    Review patient scheduling and availability

    Manage and assist with Site Opening Acceleration

    Develop key relationships and begin pre-screening activity

    Continuously increase and sharpen therapy and technical knowledge as well as presentation skills.

    Responsible for being able to conduct scientific / technical presentations and discussions on renal therapy.

    Support study and therapy awareness at site and beyond

    Keep study "Top of Mind" on site interactions

    Weekly communication and study updates

    Chart Review/Pre-Screening Logs/EMR Alerts ICD-10

    Identify patient pathways

    Track patient logs and outcome

    Proactively address barriers to recruitment

    Oversee and manage communication and reduce handoffs and redundancies

    Liaison between the site, study team, and the sponsor, to prevent fall through

    Facilitate the sharing of best practice globally

    Assumes other duties as assigned by the Supervisor.

    To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.


    qualifications:


    Bachelor's degree and a minimum of 5 years of clinical experience is required; advanced degree in a scientific discipline is preferred.

    Solid knowledge of FDA regulations for medical communications.

    Excellent presentation and teaching skills.

    Solid knowledge of good clinical practice guidelines and ability to implement

    Must be able to provide guidance and training to the team supervising regarding applicable regulatory and legal requirements and guidelines

    Solid knowledge of FDA regulations for medical communications.

    Excellent medical writing and oral communication skills.

    Solid know ledge of Acute Therapies and competitor products and therapies

    High flexibility and ability to travel

    Team-oriented.

    Self-motivated with exceptional follow through.

    Clinically skilled, licensed health care professional in Nursing, Pharmacy, or other allied health profession.

    Degree of ICU or Dialysis nurse is preferred

    Recent or ongoing work in a clinical position is desirable, as is experience in teaching/in-servicing other health care professionals.

    Minimum of 5 years clinical experience.

    Experience as therapy specialist is desirable

    skills:
    Clinical research, GCP (Good Clinical Practice)

    Equal Opportunity Employer:

    Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.


    At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants.

    If you require a reasonable accommodation to make your application or interview experience a great one, please contact


    Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc.

    In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

    Applications accepted on ongoing basis until filled.