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You will be updated with latest job alerts via email$ 70720 - 126880
1 Vacancy
The ideal candidate will have experience working with newly diagnosed patients survivors of childhood cancer and/or those with chronic illness diagnoses. Attention to detail and organizational skills are essential in coordinating data across multiple disciplines and collaborating sites.
This role will be research focused and be patient/participant facing.
CRA I Responsibilities include:
Perform data abstraction collection and entry to support clinical research.
Assist with submission for all reportable events (e.g. adverse events protocol variations).
Assist with study planning and preparation of regulatory materials.
Recruitment enrollment and evaluation of study participants.
Maintain/enter data as required for case report forms.
Ensure compliance with prescribed interventions and evaluations of the assigned protocol(s).
Provide data to the collaborating research organization (CRO) or study sponsor and prepare data reports as directed.
Delivery of inperson and telehealth interventions.
Perform other duties as assigned to meet the goals and objectives of the department and institution.
Maintains regular and predictable attendance.
CRA II Responsibilities include all the above in addition to:
Act as site study coordinator conducting informed consent process as designated and assisting with protocol submissions (internally sponsored and/or externally sponsored) for review by federal or institutional committees (e.g. CTSRC and IRB) as applicable.
Develop maintain monitor and/or share assigned/relevant documentation (e.g. investigator files case report forms study data).
Perform data abstraction collection and entry to support clinical research.
Prepare submission for all reportable events (e.g. adverse events protocol variances violations).
Prepare detailed data reports as required.
Provide patient care education and management (e.g. routine test conduct; assistance in clinical procedures; medication instruction monitoring and documentation; patient care coordination; education on protocol activities) as applicable.
CRA I Minimum Education:
Bachelors degree in relevant area required.
CRA I Minimum Experience:
Prior industry experience preferred.
CRA II Minimum Education:
Bachelors degree in relevant area required.
Masters degree preferred.
CRA II Minimum Experience:
2 years of experience in carrying out research preferably in healthcare settings.
Experience Exception: Masters degree and some experience preferred.
Experience managing crossfunctional communication including liaison between site and study teams.
Some experience with documentation and tracking systems/processes.
Proven performance in earlier role.
Compensation
In recognition of certain U.S. state and municipal pay transparency laws St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets experience and training licensure and certifications and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $70720 $126880 per year for the role of Clinical Research Associate I or II Psychology.Explore our exceptional benefits!
No Search Firms
St. Jude Childrens Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.
Required Experience:
IC
Full-Time