Clinical Research Asst 1
Plano, TX Plano, TX Full-time Full-time 3 hours ago 3 hours ago 3 hours ago Shift:
Mon - Fri 8am -5pm, some evenings & weekends necessary Location:
Legacy Plano, with travel in the Dallas area required JOB SUMMARY The All of Us Research Program (joinallofus.
org) is a nationwide initiative to enroll 1 million people who live in the United States.
Our role is to invite, 'Recruit to Retain,' and build long-term relationships with participants.
The Clinical Research Assistant will work full-time on this Research Program with the team to recruit, enroll, and retain participants.
The Clinical Research Assistant 1 assists the research team in the implementation and conduct of clinical trials per federal, state and institutional guidelines by performing delegated tasks during all phases of trials from pre-study implementation through study closure.
ESSENTIAL FUNCTIONS OF THE ROLE Coordinates implementation of various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers, and supervisors, providing in-service education for healthcare professionals, and working with Pharmacy to ensure a smooth project flow.
Assists in the development of research study budgets for new clinical trials and helps ensure that appropriate billing or charging mechanisms are in place for research charges related to research studies.
Assists and learns to coordinate research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
Assists with regulatory compliance including assisting with preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms.
Ensures that all study documents are complete and that records are retained per federal, state, and institutional standards.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences, and participating in professional organizations.
Learns to conduct audits of research studies to check the accuracy, integrity, and consistency of research studies.
Learns to coordinate study-monitoring visits.
KEY SUCCESS FACTORS Good written and oral communication skills.
Good computer skills, including Microsoft Office.
Access or other database experience preferred.
Ability to establish and maintain effective working relationships.
Ability to manage time reactive projects in order to meet deadlines.
Phlebotomy skills preferred.
BENEFITS Our competitive benefits package includes the following.
Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5% Tuition Reimbursement PTO accrual beginning Day 1 Note:
Benefits may vary based upon position type and/or level QUALIFICATIONS - EDUCATION - H.
S.
Diploma/GED Equivalent - EXPERIENCE - Less than 1 Year of Experience Coordinates implementation of various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers, and supervisors, providing in-service education for healthcare professionals, and working with Pharmacy to ensure a smooth project flow.
Assists in the development of research study budgets for new clinical trials and helps ensure that appropriate billing or charging mechanisms are in place for research charges related to research studies.
Assists and learns to coordinate research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
Assists with regulatory compliance including assisting with preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms.
Ensures that all study documents are complete and that records are retained per federal, state, and institutional standards.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences, and participating in professional organizations.
Learns to conduct audits of research studies to check the accuracy, integrity, and consistency of research studies.
Learns to coordinate study-monitoring visits.
Good written and oral communication skills.
Good computer skills, including Microsoft Office.
Access or other database experience preferred.
Ability to establish and maintain effective working relationships.
Ability to manage time reactive projects in order to meet deadlines.
Phlebotomy skills preferred.
Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5% Tuition Reimbursement PTO accrual beginning Day 1.
Estimated Salary: $20 to $28 per hour based on qualifications.
Mon - Fri 8am -5pm, some evenings & weekends necessary Location:
Legacy Plano, with travel in the Dallas area required JOB SUMMARY The All of Us Research Program (joinallofus.
org) is a nationwide initiative to enroll 1 million people who live in the United States.
Our role is to invite, 'Recruit to Retain,' and build long-term relationships with participants.
The Clinical Research Assistant will work full-time on this Research Program with the team to recruit, enroll, and retain participants.
The Clinical Research Assistant 1 assists the research team in the implementation and conduct of clinical trials per federal, state and institutional guidelines by performing delegated tasks during all phases of trials from pre-study implementation through study closure.
ESSENTIAL FUNCTIONS OF THE ROLE Coordinates implementation of various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers, and supervisors, providing in-service education for healthcare professionals, and working with Pharmacy to ensure a smooth project flow.
Assists in the development of research study budgets for new clinical trials and helps ensure that appropriate billing or charging mechanisms are in place for research charges related to research studies.
Assists and learns to coordinate research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
Assists with regulatory compliance including assisting with preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms.
Ensures that all study documents are complete and that records are retained per federal, state, and institutional standards.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences, and participating in professional organizations.
Learns to conduct audits of research studies to check the accuracy, integrity, and consistency of research studies.
Learns to coordinate study-monitoring visits.
KEY SUCCESS FACTORS Good written and oral communication skills.
Good computer skills, including Microsoft Office.
Access or other database experience preferred.
Ability to establish and maintain effective working relationships.
Ability to manage time reactive projects in order to meet deadlines.
Phlebotomy skills preferred.
BENEFITS Our competitive benefits package includes the following.
Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5% Tuition Reimbursement PTO accrual beginning Day 1 Note:
Benefits may vary based upon position type and/or level QUALIFICATIONS - EDUCATION - H.
S.
Diploma/GED Equivalent - EXPERIENCE - Less than 1 Year of Experience Coordinates implementation of various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers, and supervisors, providing in-service education for healthcare professionals, and working with Pharmacy to ensure a smooth project flow.
Assists in the development of research study budgets for new clinical trials and helps ensure that appropriate billing or charging mechanisms are in place for research charges related to research studies.
Assists and learns to coordinate research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
Assists with regulatory compliance including assisting with preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms.
Ensures that all study documents are complete and that records are retained per federal, state, and institutional standards.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences, and participating in professional organizations.
Learns to conduct audits of research studies to check the accuracy, integrity, and consistency of research studies.
Learns to coordinate study-monitoring visits.
Good written and oral communication skills.
Good computer skills, including Microsoft Office.
Access or other database experience preferred.
Ability to establish and maintain effective working relationships.
Ability to manage time reactive projects in order to meet deadlines.
Phlebotomy skills preferred.
Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5% Tuition Reimbursement PTO accrual beginning Day 1.
Estimated Salary: $20 to $28 per hour based on qualifications.
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