Research Coordinator Job at Arrow Search Partners (Boston)

Research Coordinator

The Research Coordinator provides assistance to the Principal Investigator and S...

Location

United States , Bethesda

Salary:

55000.00 - 75000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent work experience required
2-4 years’ experience in clinical research preferred
2-4 years’ non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines

Job Responsibility

Promote safety and confidentiality of research participants at all times
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol
may coordinate the collection and analysis of research data
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position
may perform aspects of research protocol, as required, in accordance with specified program objectives
Organize and facilitate meetings, conferences, and other events associated with research activities
may perform and/or coordinate outreach activities, as appropriate to research objectives

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year
up to 4 weeks of paid time off in a rolling year

Fulltime

Research Coordinator

The Research Coordinator provides assistance to the Principal Investigator and S...

Location

United States , Wright Patterson AFB

Salary:

22.00 - 28.00 USD / Hour

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent work experience required
2-4 years’ experience in clinical research preferred
Strong research skills and experience with military populations, preferred
2-4 years’ non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines
Visa sponsorship not available

Job Responsibility

Participant Coordination: Recruit, screen, and enroll military nursing personnel into the study
Serve as the primary contact for participants throughout the study
Schedule and manage weekly virtual BSS sessions, including sending Zoom.gov links
Data Management: Administer baseline and post-intervention surveys via Max.gov
Maintain a secure master list linking participant IDs to contact information
Input and manage demographic and survey data in Excel™
Compliance & Ethics: Ensure adherence to IRB protocols and consent procedures
Monitor attendance and maintain documentation for reporting
Coordinate with Chaplain facilitators and civilian team members to avoid coercion
Logistics & Communication: Liaise with internal stakeholders to manage study materials and storage

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Coverage is provided for employees and family members including domestic partners
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year

Parttime

Research Coordinator

The Research Coordinator provides assistance to the Principal Investigator and S...

Location

United States , Tacoma

Salary:

55000.00 - 65000.00 USD / Year

THE GENEVA FOUNDATION

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent work experience required
2-4 years’ experience in clinical research preferred
2-4 years’ non-profit, research, or healthcare experience desired
Demonstrate competence in oral and written communication
Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Knowledge of CFR, GCP and ICH guidelines

Job Responsibility

Promote safety and confidentiality of research participants at all times
Adhere to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and infection control procedures
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures
Plan, implement and maintain data collection and analysis systems in support of research protocol
may coordinate the collection and analysis of research data
Recruit, instruct and coordinate research subjects and/or volunteers, as appropriate to specific study objectives and work scope
Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position
may perform aspects of research protocol, as required, in accordance with specified program objectives
Organize and facilitate meetings, conferences, and other events associated with research activities
may perform and/or coordinate outreach activities, as appropriate to research objectives

What we offer

medical, dental, and vision healthcare
Flexible Spending Account
Health Savings account, with employer contribution
Short-and long-term disability
Employee Assistance Program
Life & ADD insurance
403b retirement plan with generous employer match
flexible leave options
11 paid holidays per year
up to 4 weeks of paid time off in a rolling year

Fulltime

Research Coordinator

Join Our Mission to Transform Trauma Care. As a Clinical Research Coordinator on...

Location

United States , Charlotte

Salary:

28.55 - 42.85 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Bachelor's Degree and research experience required
Master's Degree preferred
Phlebotomy certification or venipuncture skills preferred
BLS HCP certification from AHA preferred
Certification in clinical research (SoCRA, ACRP) preferred
Prior experience in clinical trials, especially drug and/or device studies, is strongly preferred
Strong communication and teamwork skills
Ability to thrive in a fast-paced, high-acuity setting
Prepared to take on leadership responsibilities as the Lead Coordinator for a high-priority, Department of Defense–funded Traumatic Brain Injury (TBI) study

Job Responsibility

Determines protocol-related needs to conduct the trial and orders supplies and equipment
Recruits and screens potential patients and obtains informed consent
Assists in providing patient education and benefits and risks of participating in a clinical drug trial
Designs organizational tools and forms to facilitate accurate data collection and recordkeeping
Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol
Manages research funds
Schedules patient visits and laboratory and diagnostic test procedures
Coordinates drug shipments, storage, and accountability with pharmacy
Coordinates with Investigational Pharmacy for subjects to receive required drugs
Reviews trends, problems encountered, patient adverse events, and patient progress

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance

Fulltime

Research Coordinator

Location

United States , New York

Salary:

100000.00 - 115000.00 USD / Year

Arrow Search Partners

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
3-5 years of administrative experience
Financial services experience preferred
Proficiency in Microsoft Office

Job Responsibility

Provide high-level administrative support including calendar management, meeting coordination, travel arrangements, and expense processing
Assist with team reporting, research distribution, and other operational tasks
Coordinate internal and external meetings with company management, research analysts, and other stakeholders
Support logistics for in-person meetings including conference room reservations and visitor coordination
Maintain internal records including meeting notes, contact databases, and research summaries

Research Coordinator

Location

United States , New York

Salary:

100000.00 - 115000.00 USD / Year

Arrow Search Partners

Expiration Date

Until further notice

Requirements

Bachelor’s degree required
3-5 years of experience as an admin or EA
Experience in financial services strongly preferred
Proficiency in Microsoft Office
Strong verbal and written communication skills with a professional demeanor

Job Responsibility

Provide high-level administrative support including calendar management, meeting coordination, travel arrangements, and expense processing
Coordinate internal and external meetings with company management, research analysts, and other stakeholders
Serve as a liaison between the investment team and external contacts
Maintain internal records including meeting notes, contact databases, and research summaries using shared platforms
Support logistics for in-person meetings including conference room reservations and visitor coordination
Assist with team reporting, research distribution, and other operational tasks

New

Clinical Research Coordinator – Neurophysiology Research Core (CNRC)

The Clinical Research Coordinator will play a primary role in collecting data fo...

Location

United States , Brookline

Salary:

44657.60 - 69773.60 USD / Year

Boston Children's Hospital

Expiration Date

Until further notice

Requirements

A Bachelor's degree is required
2 years of experience is required
Previous experience with children with autism or other neurodevelopmental conditions is ideal
Previous experience working in a research setting (preferably paid professional experience, but may include undergraduate research experiences) is also a plus.

Job Responsibility

Consents and recruits patients for research studies through personal interviews and written communications with patients/families
Provides detailed background information regarding studies to families, communicates all policies and procedures, and responds to all inquiries
Evaluates suitability of prospective study candidates and makes selections based upon clinical knowledge of each study
Performs EEG and other data collection methods (e.g., ERP, eye-tracking) on participants aged 0-65 years
Serves as liaison to the families/patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them during data collection
Acts as a resource to study participants, addressing any concerns they may have
Troubleshoots resolution of any issues that may arise during data collection
Participates in the training of newly hired research study assistants, as required
Coordinates activities between the hospital and research laboratories to ensure correct testing/processing and send out instructions specific to the study
Communicates project policies and procedures to personnel

What we offer

flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement
cell phone plan discounts
discounted rates on T-passes

Fulltime

New

Clinical Research Coordinator

Investigators in the Division of Cancer Genetics and Prevention at the Dana-Farb...

Location

United States , Boston

Salary:

48100.00 - 54400.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor's degree required, with a focus in public health, social science, or natural science preferred
0-1 years of research experience required, with experience in a clinical or scientific setting strongly preferred
Effective in working independently and as part of a team
Comfortable with patient and clinical staff interaction and handling research specimens (e.g. saliva, blood, tissue, and/or urine)
Excellent interpersonal skills and the ability to communicate and relate effectively with diverse groups
Detail-oriented with excellent organizational, communication, problem-solving, and time management skills
Strong computer skills, including proficiency with Microsoft Office products, knowledge or ability to learn other systems such as Epic and REDCap
Competencies in study data entry and/or CRF completion, research study coordination, and regulatory requirements
Dependable, motivated, and willing to learn new processes and procedures as needed
Ability to approach projects in a responsible, thoughtful, and thorough manner

Job Responsibility

Responsible for participant recruitment, data reporting and management, collection of source documents, use and development of case report forms, adverse event reporting, filing and archiving of study records, and resolution of data queries
Interact with study participants as directed/required by the protocol and/or study team
Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
Coordination and management of studies, including communication with regulatory authorities
Close-out of studies, including contributing to research articles, audit preparation, and communication with regulatory agencies
Facilitation of blood and tissue specimen collection processes, with potential travel needed to other local institutions via shuttle network

Fulltime

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