Actalent
Job Title: Clinical Research CoordinatorJob Description
We are seeking a dedicated Clinical Research Coordinator to oversee the initiation and activation of new clinical trial protocols. This role involves a combination of data management and patient interaction, ensuring the smooth operation and compliance of clinical trials.
Responsibilities
Coordinate the preparation of study tools, including study binders, medication diaries, eligibility checklists, and flow sheets.
Develop study tools using Oncore®, Excel®, and Word, in collaboration with the Research Nurse Clinician (RNC) and physicians.
Review patients' charts and medical history to confirm protocol eligibility and obtain necessary source documents.
Ensure IRB approved informed consent forms are properly obtained, signed, and documented.
Maintain research records for all patients enrolled in studies, including patient consent, eligibility, and case report forms.
Assist with grading adverse events and complete Serious/Unexpected Adverse Event forms as required.
Provide regular reports to tumor study group members and Principal Investigators using Oncore®.
Serve as a liaison with study sponsors, scheduling monitoring visits and conference calls, and responding to queries.
Essential Skills
4+ years of clinical research experience.
4+ years of oncology experience.
Experience working with multiple EDC systems, including Medidata and Inform.
Robust background in data management and coordination.
Experience in recruiting, screening, and consenting patients for clinical trials.
Blood processing experience.
Additional Skills & Qualifications
Bachelor's Degree minimum.
Experience in gynecology oncology is a plus.
Strong communication and organizational skills.
Work Environment
The position requires being on-site in the Bronx four days per week. The role involves both clinic-based work and data management, providing a dynamic and engaging work environment.
Job Type & Location
This is a Permanent position based out of bronx, NY.
Pay and Benefits
The pay range for this position is $85000.00 - $85000.00/yr.
Montefiore Perm Benefits Offered
Workplace Type
This is a hybrid position in bronx,NY.
Application Deadline
This position is anticipated to close on Nov 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
We are seeking a dedicated Clinical Research Coordinator to oversee the initiation and activation of new clinical trial protocols. This role involves a combination of data management and patient interaction, ensuring the smooth operation and compliance of clinical trials.
Responsibilities
Coordinate the preparation of study tools, including study binders, medication diaries, eligibility checklists, and flow sheets.
Develop study tools using Oncore®, Excel®, and Word, in collaboration with the Research Nurse Clinician (RNC) and physicians.
Review patients' charts and medical history to confirm protocol eligibility and obtain necessary source documents.
Ensure IRB approved informed consent forms are properly obtained, signed, and documented.
Maintain research records for all patients enrolled in studies, including patient consent, eligibility, and case report forms.
Assist with grading adverse events and complete Serious/Unexpected Adverse Event forms as required.
Provide regular reports to tumor study group members and Principal Investigators using Oncore®.
Serve as a liaison with study sponsors, scheduling monitoring visits and conference calls, and responding to queries.
Essential Skills
4+ years of clinical research experience.
4+ years of oncology experience.
Experience working with multiple EDC systems, including Medidata and Inform.
Robust background in data management and coordination.
Experience in recruiting, screening, and consenting patients for clinical trials.
Blood processing experience.
Additional Skills & Qualifications
Bachelor's Degree minimum.
Experience in gynecology oncology is a plus.
Strong communication and organizational skills.
Work Environment
The position requires being on-site in the Bronx four days per week. The role involves both clinic-based work and data management, providing a dynamic and engaging work environment.
Job Type & Location
This is a Permanent position based out of bronx, NY.
Pay and Benefits
The pay range for this position is $85000.00 - $85000.00/yr.
Montefiore Perm Benefits Offered
Workplace Type
This is a hybrid position in bronx,NY.
Application Deadline
This position is anticipated to close on Nov 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.