Research Associate 3 Job at Baptist Health (Miami)

Research Associate 3

Responsible for collecting, analyzing and interpreting collected data. The Resea...

Location

United States , Miami

Salary:

58494.88 - 76043.34 USD / Year

Baptist Health

Expiration Date

Until further notice

Requirements

Masters
Collab Inst Training Init
CITI certification required within 30 days of hire
While a Master's degree of science is a minimum requirement, candidates with PhD and MD degrees (especially those who completed their residency programs) are preferred
Candidates must be highly organized with strong analytical, research, math and statistical skills as well have had previous experience working in an academic and/or scientific setting
Minimum Required Experience: 5 Years

Job Responsibility

Responsible for collecting, analyzing and interpreting collected data
The Research Associate 3 will adhere to Baptist Health South Florida (BHSF) guidelines when presenting research outcomes and ensure that the highest quality of research is performed.

What we offer

Career growth and development opportunities, with clear pathways and ongoing support
Comprehensive health and wellness resources that go beyond traditional benefits
A wellness program that can help employees eliminate their medical plan deductible, reducing out-of-pocket healthcare costs
Tuition reimbursement to support continued learning and advancement

Fulltime

Clinical Research Associate II/Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Must be fluent in English and in the native language(s) of the country they will work in
Ability to travel 60-80%
Valid driver’s license and passport required
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock
Serve as the primary point of contact for assigned investigator sites
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel
Attend investigator meeting when required
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit
Submit all required reports, documentation, updates and tracking within required timeframes
Identify and resolve investigator site issues within required timeframes

What we offer

Career growth and development
Flexible work arrangements
Diverse therapeutic areas and project exposure
Advanced Technology

Clinical Research Associate II/Sr. Clinical Research Associate - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Must be fluent in English and in the native language(s) of the country they will work in
Ability to travel 60-80%
Valid driver’s license and passport required
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
Serve as the primary point of contact for assigned investigator sites
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with Site Care Partner to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
Provide protocol training to, and address protocol related questions from the investigator site staff when required
Attend investigator meeting when required (virtual or F2F)
Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Senior Clinical Research Associate or Clinical Research Associate II

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

United States , Blue Bell

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific or healthcare-related field
Minimum of 1-year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail
Ability to work independently and collaboratively in a fast-paced environment
Ability to travel at least 60% of the time (international and domestic - fly and drive)

Job Responsibility

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data
Contributing to the preparation and review of study documentation, including protocols and clinical study reports

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Research Associate 3, Neuro Medical Oncology

Responsible for collecting, analyzing and interpreting collected data. The Resea...

Location

United States , Miami

Salary:

58494.88 - 76043.34 USD / Year

Baptist Health

Expiration Date

Until further notice

Requirements

Masters degree
CITI certification required within 30 days of hire
While a Master's degree of Science is a minimum requirement, candidates with PhD and MD degrees (especially those who completed their residency programs) are preferred
Candidates must be highly organized with strong analytical, research, math and statistical skills as well has had previous experience working in an academic and/or scientific setting
Minimum Required Experience: 5 Years

Job Responsibility

Responsible for collecting, analyzing and interpreting collected data
Adhere to Baptist Health South Florida (BHSF) guidelines when presenting research outcomes
Ensure that the highest quality of research is performed

Fulltime

Research Associate 3, Radiation Therapy

Responsible for collecting, analyzing and interpreting collected data. The Resea...

Location

United States , Miami

Salary:

55800.78 - 72541.01 USD / Year

Baptist Health

Expiration Date

Until further notice

Requirements

Masters degree of Science minimum requirement
CITI certification required within 30 days of hire
Highly organized
Strong analytical skills
Strong research skills
Strong math skills
Strong statistical skills
Previous experience working in an academic and/or scientific setting

Job Responsibility

Collecting data
Analyzing data
Interpreting collected data
Adhere to Baptist Health South Florida (BHSF) guidelines when presenting research outcomes
Ensure that the highest quality of research is performed

Fulltime

Research Associate 3, Breast Surgical Oncology

Responsible for collecting, analyzing and interpreting collected data. The Resea...

Location

United States , Miami

Salary:

58494.88 - 76043.34 USD / Year

Baptist Health

Expiration Date

Until further notice

Requirements

Masters degree is required
CITI certification required within 30 days of hire
Candidates must be highly organized with strong analytical, research, math and statistical skills
Must have previous experience working in an academic and/or scientific setting
Minimum Required Experience: 5 Years

Job Responsibility

Responsible for collecting, analyzing and interpreting collected data
Adhere to Baptist Health South Florida (BHSF) guidelines when presenting research outcomes
Ensure that the highest quality of research is performed

Fulltime

Research Associate 3, Oncology Clinical Trials

Responsible for collecting, analyzing and interpreting collected data. The Resea...

Location

United States , Miami

Salary:

58494.88 - 76043.34 USD / Year

Baptist Health

Expiration Date

Until further notice

Requirements

Masters Degree is required
CITI certification required within 30 days of hire
Candidates must be highly organized with strong analytical, research, math and statistical skills
Previous experience working in an academic and/or scientific setting
Minimum Required Experience: 5 Years

Job Responsibility

Responsible for collecting, analyzing and interpreting collected data
Adhere to Baptist Health South Florida (BHSF) guidelines when presenting research outcomes
Ensure that the highest quality of research is performed

Fulltime

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Research Associate 3

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Research Associate 3

Research Associate 3

Clinical Research Associate II/Senior Clinical Research Associate

Clinical Research Associate II/Sr. Clinical Research Associate - Oncology

Senior Clinical Research Associate or Clinical Research Associate II

Research Associate 3, Neuro Medical Oncology

Research Associate 3, Radiation Therapy

Research Associate 3, Breast Surgical Oncology

Research Associate 3, Oncology Clinical Trials

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