Clinical Research Coordinator II Job at Solomon Page (Nashua)

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 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 II

We are seeking a motivated and experienced Clinical Research Coordinator II to s...

Location

United States , Nashua

Salary:

60000.00 - 75000.00 USD / Year

Solomon Page

Expiration Date

Until further notice

Requirements

Minimum of 3 years of direct patient-facing clinical research experience in industry-sponsored, interventional drug trials
Ophthalmology experience (Technician or Ophthalmology CRC background)
Strong patient communication skills with the ability to build trust and support retention
Experience with patient care, recruitment, lab specimen handling, monitoring, and audits
Excellent organizational, multitasking, and time management skills
Willingness and ability to travel regularly (up to 50%)

Job Responsibility

Coordinate day-to-day clinical trial activities across multiple therapeutic areas, including ophthalmology, dermatology, and pulmonology
Support studies at headquarters and satellite site locations
Conduct patient-facing activities, including informed consent, visit scheduling, and follow-up
Manage patient recruitment and enrollment through database reviews, outreach, pre-screening, and ongoing communication
Perform blood draws and manage biospecimen processing and shipping per protocol
Maintain accurate study documentation, source data, and regulatory binders across CTMS, EDC, and other systems
Support monitoring visits and participate in internal and external audits
Serve as a key liaison between sponsors, CROs, investigators, and internal teams
Provide cross-functional support as needed to meet study timelines and goals

What we offer

medical
dental
401(k)
direct deposit
commuter benefits

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 - Precision Medicine

A Clinical Research Coordinator II (CRC II) position is available for the Precis...

Location

United States , BOSTON

Salary:

56000.00 - 63700.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

bachelor's degree or 2 years of experience as a Dana-Farber Clinical Research Coordinator
1-3 years of relevant experience
preference for those with a background in medical or scientific research or a technology-oriented business environment
excellent organization and communications skills
strong interpersonal skills
detail oriented
ability to effectively manage time and prioritize workload
must practice discretion and adhere to hospital confidentiality guidelines
computer skills including the use of Microsoft Office

Job Responsibility

liaise between the LSP, DF/HCC hospitals, and external investigators to facilitate highly collaborative translational biomarker driven research
facilitate the emerging fields of cancer spatial biology
work closely with principal investigators, program managers, biomarker researchers, and data scientists
primary data collection and management of patient clinical information as it pertains to participation in clinical trials and patient consent
ensure timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities
support and maintain participant/subject trial binders and maintain regulatory binders
ensure study compliance with all state, federal, and IRB requirements
screen patients for protocol eligibility
obtain informed consent for non-treatment trials
register study participants with the clinical trials management system, ONCORE

Fulltime

Clinical Research Coordinator II-OB/GYN

Under minimal supervision, coordinates the clinical assessments of the study sub...

Location

United States , New York

Salary:

63653.84 - 85000.06 USD / Year

Mount Sinai Health System

Expiration Date

Until further notice

Requirements

Bachelors degree in sciences or related field
2 years of clinical research

Job Responsibility

Analyzes moderately complex clinical research data
Assists in interpreting clinical research data
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects
Prepares and ensures grant applications, IRB/GCO documents are submitted
Ensures accurate and complete compilation of subject data through chart reviews
Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials
Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests
Independently obtains informed consent for other clinical studies
Mentors Clinical Research Coordinators in training
Performs other related duties

Clinical Research Nurse II – Oncology

Assists with clinical and operational management of research protocols • Impacts...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

AS
BS
Clinical Research Experience
Clinical Experience
Registered Nurse (RN) - State Nursing Boards
Driver's License - DMV

Job Responsibility

Assists with clinical and operational management of research protocols
Impacts research throughout the Baptist Health Systems-Research
Effectively conducts assigned operations of research protocols
Coordinates, evaluates, and follows patient participation in clinical trials
Assists in the collection and evaluation of data
Under direction, performs protocol-specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens and monitoring responses
May administer medications
Provides patient and family education
May provide professional and ancillary staff education concerning research protocols as required
Other duties as assigned

Fulltime

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Clinical Research Coordinator II

Job Description

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