Research & Knowledge Coordinator Job at Beacon Hill (Boston)

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

Clinical Research Coordinator II

Job Description Must have RN licensure to qualify. PURPOSE AND SCOPE: Responsi...

Location

United States , Tupelo

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Graduate of a technical program in healthcare, specifically as a Registered Nurse
2 to 4 years of nursing experience, specifically as a Registered Nurse
Has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Research experience preferred
Critical care, nephrology and/ or cardiac nursing experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study's timeline of activities
Regularly evaluates the study subjects' condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

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

Float Clinical Research Coordinator II

Must be comfortable with 80% travel. Highly prefer someone who lives in the Nort...

Location

United States

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

2 to 4 years of clinical research experience
or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance
critical care, nephrology and/or cardiac experience desirable
willing to pursue CCRC or CCRP certification when eligible
current state licensure, if applicable
good computer skills: Microsoft Office
excellent communication and organizational skills
ability to work independently, and exhibit diplomacy and problem solving skills

Job Responsibility

Assists with determination of guidelines for collection of clinical data
coordinates all aspects of study subject care
protects rights and well-being of subjects
ensures thorough protocol-based study subject education
develops processes for monitoring study subjects
evaluates study subjects' condition and communicates concerns
accurately documents study subject activities
maintains documents according to HIPAA and regulatory requirements
implements study-specific quality goals
acts as point of contact for protocol compliance

Clinical Research Coordinator II

Responsible for the collection, accuracy and validity of clinical research data ...

Location

United States , Denver

Salary:

59000.00 - 100000.00 USD / Year

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Graduate of a technical program in healthcare, AA in Life Sciences or other health related field
2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
Critical care, nephrology and/ or cardiac nursing experience desirable
Willing to pursue CCRC or CCRP certification when eligible
Current state licensure, if applicable
Good computer skills: Microsoft Office minimally
Excellent communication and organizational skills
Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role

Job Responsibility

Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
Protect the rights and the well-being of subjects enrolled in studies
Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
Develops processes for methodically monitoring the status of study subjects as they progress through the study’s timeline of activities
Regularly evaluates the study subjects’ condition and communicates/documents concerns to PI to ensure subject safety
Accurately documents study subject activities as outlined by the protocol
Maintains documents according to applicable HIPAA and regulatory requirements
Implements study-specific quality goals and practices
Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance

What we offer

Medical insurance
Dental insurance
Vision insurance
401(k) with company match
Paid time off
Parental leave

Fulltime

Clinical Research Coordinator II

This role requires 100% travel. PURPOSE AND SCOPE: Works under the supervision o...

Location

United States , Las Vegas

Salary:

Not provided

Fresenius Kidney Care Eupora

Expiration Date

Until further notice

Requirements

Bachelor's Degree or an equivalent combination of education and experience
Graduate of a technical program in healthcare (e.g. LVN/LPN, Medical Assistant or Dialysis Technician) AA in Life Sciences or other health related field
2 to 5 years' healthcare experience with Dialysis experience preferred
Research experience preferred
Willing to pursue CCRC or SoCRA certification when eligible
Current appropriate state licensure if applicable
Proficient with PCs and Microsoft Office applications
Good communication and organizational skills
Ability to work independently

Job Responsibility

Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with FDA, GCP, and ICH Guidelines
Under the supervision of the Principal Investigator (PI) and appropriate management prepares and submits regulatory documents in an accurate and timely manner
In collaboration with the PI, incorporates clinical judgment and knowledge of protocol to identify potential study participants according to inclusion and exclusion criteria
Obtains informed consent according to GCP
Schedules subject visits
Prepares labs/tests per protocol
Responsible for study drug storage and drug accountability according to the parameters of the study protocol and sponsor requirements
Administers the investigational product according to the parameters of the study protocol and under the direction of the physician
Monitors and evaluates patients' condition with regard to the investigational product
Consults with PI regarding the appropriate administration of investigational product

What we offer

Healthcare
Continuing Education
Paid Time Off
Collaborative Environment
Additional Perks
401(k) Retirement Saving

Fulltime

Clinical Research Coordinator

We are looking for a Clinical Research Coordinator to support clinical research ...

Location

United States , Anaheim

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

At least 2 years of relevant experience, including a minimum of 1 year working in a Clinical Research Coordinator or closely related clinical research role
High school diploma or equivalent required
a bachelor's degree is preferred
Working knowledge of regulations and ethical standards governing human subject research and clinical trial conduct
Ability to manage scheduling, administrative support tasks, and detailed documentation in a fast-paced research setting
Strong verbal and written communication skills with the ability to interact professionally across teams and with external partners
Demonstrated problem-solving skills, sound judgment, and composure when responding to urgent or unexpected situations
Comfortable working independently while also contributing effectively within a collaborative team environment
Proficiency with Microsoft applications and general administrative coordination tools

Job Responsibility

Coordinate participant-related study activities from enrollment through closeout, helping keep each trial on schedule and aligned with approved protocols
Maintain organized research records, track study documentation, and support accurate preparation of materials required for clinical trial operations
Arrange visits, assessments, and data collection appointments while ensuring timelines are followed and information is recorded appropriately
Monitor study participants during assigned activities and assist with compiling research findings, summaries, and required reports
Record adverse events, protocol departures, and unexpected study issues in a timely manner to support regulatory compliance and quality standards
Assist with administrative and regulatory tasks tied to active studies, including maintaining files and supporting protocol-related processes
Provide clear explanations to prospective participants and caregivers regarding study expectations, procedures, and visit requirements
Perform protocol-directed procedures such as vital signs, EKGs, blood draws, and other assigned safety or efficacy assessments
Collaborate with research staff and leadership on additional study development or coordination activities as needed

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

Clinical Research Coordinator

CRC monitors and coordinates multiple research projects in order to assess the n...

Location

United States , Madera

Salary:

35.85 - 53.35 USD / Hour

Valley Children's Healthcare

Expiration Date

Until further notice

Requirements

Equivalent Experience Three (3) years research experience (required)
College Degree - 4 year (preferred)
CCRP - Certified Clinical Research Professional - SOCRA - Society of Clinical Research Associates (preferred)
Minimum one (1) year Research (required)
Minimum two (2) years Related experience (preferred)
Experience with clinical trials is strongly preferred
Knowledge of Institutional Review Board (IRB) policies and procedures
Knowledge of the scientific method and statistical analysis techniques preferred
Computer Skills Microsoft Office

Job Responsibility

Monitor and coordinate multiple research projects
Assess the need for and implement strategies to ensure the conduct of quality research
Achievement of expected timelines and deliverables and efficient use of resources
Assist PIs with study protocol development, ICFs, and required study documents in preparation for IRB submission
Assist with recruitment activities, consents patients, ensures eligibility prior to enrollment, and randomizes patients to study
Abstract data, complete case report forms and maintain research record and data integrity
Schedule and meet with study monitor for site visits
Maintain data in an audit ready state
Ensure study meets the requirements of executed contract and budget
Ensure compliance to the research protocol, appropriate SOPs, policies and federal regulations

Fulltime

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Research & Knowledge Coordinator

Job Description

Job Responsibility

Requirements

What we offer

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