Clinical Research Coordinator II Job at Solomon Page (Nashua)

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 Coordinator II

A Clinical Research Coordinator II opportunity with a growing research network c...

Location

United States , Los Angeles

Salary:

45000.00 - 85000.00 USD / Year

Solomon Page

Expiration Date

Until further notice

Requirements

Minimum 3+ years of clinical research experience (interventional studies preferred)
Strong communication, organization, and multitasking skills
Phlebotomy experience and Spanish fluency are a plus
Based in Los Angeles or Las Vegas

Job Responsibility

Manage day-to-day coordination of industry-sponsored clinical trials
Oversee patient recruitment, informed consent, and visit scheduling
Handle biospecimen collection and processing
Maintain regulatory documentation across CTMS and EDC platforms
Requires 50% nationwide travel to support multiple study sites
Collaborate closely with sponsors, CROs, and investigators

What we offer

medical
dental
vision
401(k)
telehealth services
ESOP
commuter benefits

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%) and on site when not traveling

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

Clinical Research Project Manager

The Clinical Research Project Manager II manages day-to-day coordination and ove...

Location

United States , Boston

Salary:

97770.00 - 103345.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor's degree in a field relevant to clinical research
Five (5) years of experience in clinical research or project management, with a focus on multi-center oncology trials, including specific experience in clinical trial operations and coordination
In-depth understanding of clinical trial phases and multi-center trial coordination, including specific requirements for PI-initiated trials
Knowledge of advanced regulatory requirements and compliance standards, with expertise in Good Clinical Practice (GCP) and FDA regulations
Familiarity with project management methodologies and strategic planning, tailored to clinical trial environments
Advanced organizational skills to manage multiple complex projects simultaneously
Strong leadership and team coordination skills to guide research teams
Proficient in developing project plans and tracking systems, utilizing clinical trial management software such as EPIC and OnCore
Ability to work independently with minimal supervision
Capability to develop and implement strategic project management solutions

Job Responsibility

Oversee the coordination, execution, and management of several Phase I, II, III PI-Initiated/Multi-Center oncology trials within the Clinical Trials Office, ensuring compliance with clinical trial regulations
Collaborate with senior managers to develop comprehensive project plans that provide direction, expectations, and milestones for participating sites
Collaborate with the Principal Investigator (PI) to develop protocols and consent forms for initial applications and amendments
Ensure the project team meets all deadlines and maintains ongoing relationships with the research team, Principal Investigators, and external collaborators
Develop systems, tools, and infrastructure for clinical trial management activities, including study start-up, site activation, research staff training, regulatory submissions, and event tracking
Prepare and present detailed status reports to key stakeholders, including information about project timelines, progress, and compliance with regulatory standards

Fulltime

Clinical Project Manager

Permanent position available immediately located in Paris. The role involves lea...

Location

France , Paris

Salary:

Not provided

AB SCIENCE

Expiration Date

Until further notice

Requirements

Holder of additional training in methodology (CESAM, IUD, …)
Successful experience of Clinical Project Manager in a pharmaceutical company or CRO
6-8 year’s experience in clinical development (Phase II and III)
Experience in oncology or autoimmune inflammatory diseases would be a plus
Experience in international development required
Experience of the regulatory environment for clinical trials
Experience of writing research reports and FDA regulatory dossiers (IND, NDA) and EMA
Fluent in English

Job Responsibility

Design, implementation and coordination of clinical studies with the support of Clinical Operations, Pharmacovigilance, Biometrics and Medical Writing
Plan the clinical development program
Prepare studies protocols, amendments and reports
Prepare regulatory dossiers
Manage relationships with investigators and opinion leaders

What we offer

Salary and package to define according to skills and experience

Fulltime

New

Clinical Research Associate I or II

Clinical Research Associate I or II - São Paulo (FSP - Sponsor Dedicated). ICON ...

Location

Brazil , São Paulo

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in English
Good social skills enabling you to deal with queries in a timely manner
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license

Job Responsibility

Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements

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

Fulltime

New

Clinical Research Associate II

Clinical Research Associate II - France - Remote. ICON plc is a world-leading he...

Location

France , Paris

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Minimum 24 months' experience as a CRA within the pharmaceutical industry or a CRO
Excellent organization skills
Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
Strong IT skills
Strong communication with the ability to multitask and work effectively under pressure
Fluency in French and professional proficiency in English

Job Responsibility

Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

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

Fulltime

Medical Appeals/Grievance Specialist II - Registered Nurse

Responsible for utilizing clinical acumen and managed care expertise related to ...

Location

United States , Phoenix

Salary:

Not provided

Blue Cross Blue Shield of Arizona

Expiration Date

Until further notice

Requirements

1 year experience in clinical and health insurance or other healthcare related field
3 years experience in clinical and health insurance or other healthcare related field AND 1 year Managed care experience with a focus in Utilization Management (UM), Prior Authorization (PA), Claims, Case Management and/or Medical Appeals and Grievance (MAG)
5 years experience in clinical and health insurance or other healthcare related field AND 2 years Managed care experience with a focus in Utilization Management (UM), Prior Authorization (PA), Claims, Case Management and/or Medical Appeals and Grievance (MAG)
8 years experience in clinical and health insurance or other healthcare related field AND 3 years above satisfactory job performance in the managed care environment with a focus in Utilization Management (UM), Prior Authorization (PA), Claims, Case Management and/or Medical Appeals and Grievance (MAG)
Associate’s Degree in a healthcare field of study or Nursing Diploma
Active, current, and unrestricted license to practice in the State of Arizona (a state in the United States) or a compact state as a Registered Nurse (RN), a Physical Therapist (PT) or a Licensed Master Social Worker LMSW.
Intermediate PC proficiency
Intermediate skill using office equipment, including copiers, fax machines, scanner and telephones
Maintain confidentiality and privacy
Advanced clinical knowledge

Job Responsibility

Perform in-depth analysis, clinical review and resolution of provider appeals/inquiries, corrected claims and subscriber reconsiderations, member appeals, corrected claims and provider grievances for all lines of business
Identify, research, process, resolve and respond to customer inquiries primarily through written / verbal communication.
Respond to a diverse and high volume of health insurance appeal related correspondence on a daily basis.
Analyze medical records and apply medical necessity criteria and benefit plan requirements to determine the appropriateness of appeal, grievance and reconsideration requests.
Maintain complete and accurate records per department policy.
Meet quality, quantity and timeliness standards to achieve individual and department performance goals as defined within the department guidelines and required by State, Federal and other accrediting organizations.
Demonstrate ability to apply plan policies and procedures effectively.
Consult and coordinate with various internal departments, external plans, providers, businesses, and government agencies to obtain information and ensure resolution of customer inquiries.
Attend staff and interdepartmental meetings.
Participate in continuing education and current developments in the fields of medicine and managed care.

Fulltime

Clinical Research Coordinator II

Solomon Page

Location:
United States , Nashua

Category:
-

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 10, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Clinical Research Coordinator II

Clinical Research Coordinator II-OB/GYN

Clinical Research Coordinator II

Clinical Research Coordinator II

Clinical Research Project Manager

Clinical Project Manager

Clinical Research Associate I or II

Clinical Research Associate II

Medical Appeals/Grievance Specialist II - Registered Nurse

Clinical Research Coordinator II

Solomon Page

Location:United States , Nashua

Category:-

Contract Type:Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:January 10, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Clinical Research Coordinator II

Clinical Research Coordinator II-OB/GYN

Clinical Research Coordinator II

Clinical Research Coordinator II

Clinical Research Project Manager

Clinical Project Manager

Clinical Research Associate I or II

Clinical Research Associate II

Medical Appeals/Grievance Specialist II - Registered Nurse

Location:
United States , Nashua

Category:
-

Contract Type:
Employment contract

Job Posted:
January 10, 2026