Research Associate 3 Job at Baptist Health (Miami)

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

Clinical Research Associate

The Clinical Research Associate (Monitor) is responsible for supporting clinical...

Location

Salary:

Not provided

HonorVet Technologies

Expiration Date

Until further notice

Requirements

B.S. or B.A. and/or an equivalent combination of education or experience
Minimum of 3 years of experience directly related to the execution of clinical research studies
Available to travel (up to 60%) on short notice and independently manage travel schedules
Must have analytical skills, be detail oriented and have good interpersonal skills
Knowledge of agency guidelines and requirements
Effective written and verbal communication skills
Ability to communicate at all levels of an organization
PC skills
word processing, spreadsheet, database, Internet search and utilization
Flexible and able to work in a fast-paced environment

Job Responsibility

Collaborate with team members in the evaluation and establishment of clinical study sites by performing site qualification visits and site initiation visits to ensure applicability of sites for planned study according to application regulatory requirements
Collaborate with Senior Clinical Research Associate to create source documentation/CRFs in alignment with protocol requirements
Collaborate with sites and internal stakeholders to align and implement site specific language for each consent/assent and support Institutional Review Board (IRB) submissions
Train site staff on protocol requirements, source documentation, and case report form completion
Conduct regular monitoring visits to ensure study protocol compliance, primary data collection is recorded properly, and appropriate reporting is being conducted
Conduct clinical study site close-out visits and ensure site files are complete, accurate and up to date
File site related documents real-time to ensure Trial Master Files are complete and accurate at all times
Provide study specific information and support report validation activities as requested for clinical study reports
Participates in team meetings and document meeting minutes and tracks action items
Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines

Equity Research Senior Associate

The successful candidate will join the Citi Research’s Global Research Center in...

Location

India , Mumbai

Salary:

Not provided

Citi

Expiration Date

Until further notice

Requirements

Prior equity research experience of 3-5 years
Relevant work-experience in the Retail and Consumer Internet sector
Strong financial modeling skills, including full company modelling experience
Good data management and analysis skills and a high degree of comfort with Excel
Strong interpersonal skills for dealing with overseas colleagues
Ability to work under pressure, with minimal supervision, and in a team environment
Highly detail-oriented and possess strong organizational skills
Pragmatic "self-starter" who can work both independently and as part of a team

Job Responsibility

Creation and maintenance of excel models for companies under coverage
Creation and maintenance of excel models for industry sub-sectors
Tracking of sector news and analysis of periodic statistical data
Constant collaboration / information exchange with fellow associates
Background analysis as a part of active research on a company / theme
Maintenance of research products such as Dailies, preview notes and results notes
Completion of ad hoc client requests, often to deadlines
Assistance in initiation of coverage on new stocks
Support in developing new products

Fulltime

Associate Medical Director

Associate Medical Director, Oncology. ICON plc is a world-leading healthcare int...

Location

Poland , Warsaw

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Medical degree (MD) required
Board certification preferred in oncology/haematology
Minimum of 3 years of experience in clinical research or medical affairs within the pharmaceutical or biotechnology industry
Strong understanding of clinical trial design, execution, and regulatory requirements
Experience in immune oncology
Excellent communication and relational skills
Demonstrated leadership and problem-solving abilities

Job Responsibility

Collaborating with cross-functional teams to design clinical development plans and study protocols
Providing medical oversight and guidance throughout the lifecycle of clinical trials
Ongoing medical review of data, supporting Safety Review Committees
Interpreting complex medical and clinical trial data to support decision-making and regulatory submissions
Contributing to the development of scientific publications, presentations, and regulatory documents
Building and maintaining relationships with investigators, key opinion leaders and regulatory authorities

What we offer

Various annual leave entitlements
A range of health insurance offerings
Competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks
Life assurance
Flexible country-specific optional benefits

Tax Senior Associate

Serve as the engagement lead on specific client accounts, take responsibility fo...

Location

United States , Oak Brook

Salary:

95000.00 - 115000.00 USD / Year

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor's degree in Accounting
Master's in Tax is a plus
Must have experience preparing and reviewing the following types of tax returns: Passthrough entity tax returns including 1065 & 1120-S
CPA, LLM or JD is preferred
3+ years of tax experience
Strong tax research skills
Excellent communication and presentation (verbal and written) skills, as well as exceptional client service skills
Proven competence with MS Office and tax compliance and research software, including ProSystem, BNA portfolio and projection, CCH Axcess, and RIA

Job Responsibility

Serve as the engagement lead on specific client accounts
Take responsibility for pre-engagement planning, execution, and final deliverables
Writing memos and tax alerts
Assist with internal and external presentations
Develop detailed engagement work plans
Illustrate budgets and schedules
Actively participate in proposals
Researching complex federal income tax law
Learn about and provide insight on new and complex tax provisions across all federal income taxes
Create tax models and checklists to be used by other members of the federal tax team

What we offer

medical
vision
dental
life
disability insurance
higher bonus structures
work from home flexibility
prioritization for employee work/life balance
fast-track career growth opportunity
401(k) plan

Fulltime

Tax Senior Associate

A high-end firm that was just rated one of the top places to work in Chicago jus...

Location

United States , Chicago

Salary:

95000.00 - 115000.00 USD / Year

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor's degree in Accounting
Master's in Tax is a plus
Must have experience preparing and reviewing the following types of tax returns: Passthrough entity tax returns including 1065 & 1120-S
CPA, LLM or JD is preferred
3+ years of tax experience
Strong tax research skills
Excellent communication and presentation (verbal and written) skills, as well as exceptional client service skills
Proven competence with MS Office and tax compliance and research software, including ProSystem, BNA portfolio and projection, CCH Axcess, and RIA

Job Responsibility

Serve as the engagement lead on specific client accounts
Take responsibility for pre-engagement planning, execution, and final deliverables
Writing memos and tax alerts
Assist with internal and external presentations
Develop detailed engagement work plans
Illustrate budgets and schedules
Actively participate in proposals
Researching complex federal income tax law
Learn about and provide insight on new and complex tax provisions across all federal income taxes
Create tax models and checklists to be used by other members of the federal tax team

What we offer

medical
vision
dental
life
disability insurance
higher bonus structures
work from home flexibility
prioritization for employee work/life balance
fast-track career growth opportunity
401(k) plan

Fulltime

Litigation Associate

We are offering an exciting opportunity with a suburban law firm in the Minneapo...

Location

United States , Maple Grove

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Possess a Juris Doctor degree from an accredited law school
Must be admitted to practice law in Minnesota
A minimum of 3 years of experience in a law firm or in-house legal team, with a focus on litigation
Excellent research skills with the ability to analyze complex legal documents

Job Responsibility

Managing legal procedures with a focus on civil litigation
Utilizing case management software to track and manage cases effectively
Preparing and briefing documents to ensure they are ready for review
Conducting depositions to gather necessary information and evidence
Handling motion practice as part of the litigation process
Ensuring all client and case details are accurately recorded and updated
Resolving client inquiries promptly and professionally
Monitoring client accounts and initiating appropriate actions when needed
Collaborating with other team members to ensure smooth case progression

What we offer

Health
Dental Insurance
Long-term Disability
Life Insurance
401(k)

Fulltime

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

Baptist Health

Location:
United States , Miami

Category:
Nursing

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
May 16, 2026

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