Clinical Trial Manager
Eliassen Group
Clinical Trial Manager
Anywhere
Type: Consulting
Category: Clinical Ops
Industry: Life Sciences
Workplace Type: Remote
Reference ID: JN -082026-108196
Date Posted: 08/05/2026
Shortcut:
Description
Recommended Jobs
Description:
Remote
Our client seeks three Clinical Trial Managers to join an established Clinical Operations FSP program. The CTM will oversee assigned clinical trials with a focus on vendor and CRO management, study execution, and financial and milestone tracking. The role ensures compliance with ICH GCP, regulations, protocols, and SOPs while collaborating with internal teams, clinical sites, and external partners. The CTM reports to Clinical Operations leadership and may support one or multiple studies across clinical operations activities.
Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.
Rate: $115000.00 to $120000.00/hr. w2
Responsibilities:
Manage all aspects of clinical trials including vendor management, CRO oversight, and coordination of study service providers.
Lead or support cross-functional study teams with focus on Clinical Operations deliverables and study execution.
Track and report study milestones, metrics, and timelines to leadership.
Ensure studies adhere to ICH GCP, applicable regulations, protocols, and SOPs.
Assist in preparation and review of clinical trial documents including protocols, informed consent, monitoring plans, project plans, CRFs, and study reports.
Partner with eTMF team to establish and maintain TMF with periodic reviews.
Coordinate and support resolution of audit findings and maintain audit-ready documentation.
Participate in service provider selection and outsourcing activities.
Identify and resolve clinical project issues and contribute to process improvements.
Assess operational feasibility, recommend study execution plans, and support site selection.
Negotiate and finalize site contracts and budgets.
Perform and manage ongoing data review.
Oversee site visits including qualification, initiation, monitoring, and close-out as needed.
Review monitoring reports to ensure quality and resolve site issues.
Track and review protocol deviations and assess impact on data.
Review and approve clinical invoices against approved scopes of work.
Forecast and oversee clinical supplies including study drug and materials.
Provide service provider oversight, identify issues, and escalate as appropriate.
Experience Requirements:
Bachelor’s degree with 3 to 5 years of experience in core clinical operations functions such as trial management, site management, and monitoring oversight.
Strong communication skills.
Self-motivated with ability to prioritize, shift, and manage multiple tasks in a fast-paced environment.
Residence in Eastern or Central time zones.
Recruitment Transparency Notice
Eliassen Group values transparency in our recruitment practices. Please be advised that Eliassen Group utilizes artificial intelligence (AI) tools as part of its initial application screening and hiring process. You may receive email and SMS notifications from the Eliassen Virtual Recruiting Team ( View email address on click.appcast.io , View phone number on click.appcast.io) inviting you to complete a brief voice screening as part of your application process. These tools assist our hiring teams in different ways, including but not limited to, assistance in reviewing application materials to help identify candidates whose qualifications most closely match the requirements of the position. All AI-assisted evaluations and responses are reviewed by human recruiters before any hiring decisions are made. The use of AI in our process is intended to support fairness, efficiency, and consistency, and Eliassen Group takes measures to prevent bias or discrimination in connection with its hiring practices. By proceeding, you acknowledge, agree, and consent to Eliassen Group’s use of these tools, including AI tools, as part of the application and hiring process.
Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.
W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.
If anyone reaches out to you about an open position connected with Eliassen Group, please ensure that you are working directly with us by confirming the following:
· When you work with Eliassen Group, all email communication will come from an Eliassen.com address, never Gmail, Yahoo, etc.
· Eliassen Group will never ask you for personal information (home address, bank account, or check routing number) until you have worked with someone clearly associated with Eliassen Group.
If you have any indication of fraudulent activity, please contact View email address on click.appcast.io .
About Eliassen Group:
Eliassen Group is a strategic consulting firm that helps organizations reach further and achieve more through our technology, business advisory, and life sciences solutions. For nearly 40 years, we have combined exceptional people, deep domain expertise, and intelligent capabilities to expand our clients’ capacity and accelerate meaningful outcomes. We are driven by a purpose to positively impact the lives of our employees, clients, consultants, and the communities we serve.
Eliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affirmative Action Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.
Don’t miss out on our referral program! If we hire a candidate that you refer us to then you can be eligible for a $1,000 referral check!
- ...Clinical Trial Manager Anywhere Type: Consulting Category: Clinical Ops Industry: Life Sciences Workplace Type: Remote Reference ID: JN -082026-108196 Date Posted: 08/05/2026 Shortcut: Description Recommended Jobs Description:...SuggestedHourly payPermanent employmentFull timeLocal areaRemote workShift work
- A leading academic medical center in Columbus, OH is seeking a Clinical Research Manager to oversee clinical trials and manage a research team. The role requires a Bachelor's Degree and 5 years of clinical research experience along with ACRP or SOCRA certification. Ideal...Suggested
- ...) seeks an energetic and collaborative applicant to serve as a Clinical Research Coordinator (CRC). The CSOR is part of the Center for... ...of surgical care for children. Job Description Summary: Manages elements of a clinical study in order to meet all protocol obligations...SuggestedTraineeshipFlexible hoursWeekend workAfternoon shift
- ...communities. Job Description Summary: The Clinical Research Coordinator works in... ...oversees the enrollment of the clinical trial as directed by the PI. Ensures that study... ...teamwork characteristics. Ability to manage time, prioritize and follow up on projects...SuggestedLocal areaRemote workShift work
- ...Clinical Research Coordinator The Behavioral Trials Office (BTO) works with investigators and research teams throughout the Abigail Wexner Research Institute... ...activities such as study start-up, day to day management, and study closure activities. The position requires...SuggestedZero hours contractWork at officeFlexible hoursWeekend workAfternoon shift
$50k - $52k
...Research Team! Centricity Research is one of North America's largest clinical research networks and a fully centralized Integrated Research Organization (IRO). We conduct Phase I-IV clinical trials across more than 35 therapeutic areas, partnering with leading...Full timeImmediate startMonday to FridayFlexible hours- Nationwide Children's Hospital in Columbus, Ohio is seeking a skilled Clinical Research Coordinator to manage clinical studies. Candidates should have at least an Associate’s Degree, with a preference for a Bachelor’s Degree, and certifications such as CNA or LPN. The role...
- Nationwide Children’s Hospital in Columbus, OH, is seeking a Clinical Research Coordinator to manage clinical study activities in line with ICH/GCP and SOPs. You will recruit, enroll and consent participants, collect data, and coordinate visits with the PI and hospital...
- A major healthcare institution in Columbus, Ohio, is seeking a Clinical Research Assistant to support the Total Cancer Care Program by managing patient informed consent and analyzing clinical research data. Qualified candidates will hold a relevant bachelor's degree and...
- Nationwide Children’s Hospital in Columbus, OH seeks a Clinical Research Coordinator to manage elements of clinical studies in line with ICH/GCP and SOPs. You will recruit, consent, enroll, and monitor subjects, ensure regulatory compliance, and maintain study data and...
- A prominent medical institution in Columbus, Ohio, is seeking a Clinical Research Coordinator to manage daily clinical research activities adhering to protocols. The role involves assessing patient eligibility, recruiting participants, and ensuring compliance with regulatory...
- 10 Nationwide Children's Hospital in Columbus, Ohio, is looking for a Clinical Research Coordinator to manage various aspects of clinical studies. Responsibilities include recruiting and enrolling subjects, ensuring compliance with regulations, collecting and managing research...
- Centricity Research in Columbus, Ohio is seeking an experienced Clinical Research Coordinator I to join our onsite team. This hands-on role conducts participant visits, adheres to protocols, and ensures data quality and timely documentation. You will partner with Investigators...
- ...and update (if necessary) the information in your candidate profile as it will transfer to your application. Job Title: Clinical Research Coordinator-Hematology Department: Medicine | IM Hematology Clinical Research Coordinator responsible for the...Shift workDay shift
- ...Clinical Research Coordinator - Oncology The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office (CTO) within the Comprehensive Cancer Center at The Ohio State University...Full timeWork at officeVisa sponsorshipWork visaShift workDay shift
- ...Overview: Summary: Manages elements of a clinical study to meet protocol obligations while following ICH/GCP guidelines and departmental/institutional... ...: Understanding of medical terminology and clinical trials preferred. Working knowledge of PCs and word processing...Full timeLocal areaFlexible hours
- Job Title Clinical Research Coordinator - Neurology Department Medicine | Neurology Job Description Summary Clinical Research Coordinator... ...by the College of Medicine (COM) Center for Clinical Research Management (CCRM) the Department of Neurology/ Division of Parkinson's...Shift workDay shift
- Clinical Research Coordinator - CCC | Clinical Trials Office Department: Clinical Trials Office, Comprehensive Cancer Center Position Summary: The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered...Work at officeShift workDay shift
- ...Workday to use the internal application process. Job Title: Clinical Research Coordinator - Neurology Department: Medicine | Neurology... ...administered by the non-cancer Center for Clinical Research Management for the Huntington's Clinical Research Division in the Department...Shift workDay shift
- Overview:Job Description Summary:Manages elements of a clinical study to meet all protocol obligations while following ICH/GCP guidelines and standard operating procedures. Includes elements such as start-up activities, launch activities, day-to-day management, and study...Flexible hours
- Nationwide Children's Hospital in Columbus, OH is seeking a Clinical Research Coordinator to manage elements of a clinical study, ensuring protocol obligations and ICH/GCP compliance. You will handle start-up, enrollment, data collection and study closure under SOPs. The...Weekend workAfternoon shift
- The Ohio State University is seeking a Clinical Research Coordinator in Neurology to coordinate daily clinical research activities within the College of Medicine's Center for Clinical Research Management and Department of Neurology. The role involves patient screening,...
- A leading higher education institution seeks a Clinical Research Coordinator in Columbus, Ohio. This role involves coordinating clinical research activities, recruiting patients, and ensuring compliance with protocols. Candidates should possess a Bachelor's Degree in biological...Day shift
- ...Columbus, Ohio is seeking a dedicated individual to coordinate clinical research activities in Body MRI and Women's Imaging. Ideal candidates... ...clinical research experience. Responsibilities include managing study data and ensuring compliance with regulatory standards. A...Afternoon shift
- Job Description Summary Manages elements of a clinical study to meet all protocol obligations while following ICH/GCP guidelines and departmental/institutional standard operating procedures. Responsibilities include start‑up, launch, day‑to‑day study management, and study...
- Ohio State University is seeking a Clinical Research Coordinator (HS) in Neurology to coordinate daily clinical research activities within the Department of Neurology. Responsibilities include identifying eligible patients, recruiting and enrolling participants, obtaining...
- The Ohio State University is seeking a Clinical Research Coordinator for Hematology in Columbus. This role focuses on coordinating observational studies, screening patients for eligibility, obtaining informed consent, and ensuring data quality across the division of Hematology...
- Berger Health System in Columbus, Ohio seeks a Clinical Research Coordinator to collaborate with the Principal Investigator and oversee... ...will be responsible for participant recruitment, data management, and ensuring compliance with GCP guidelines. Ideal candidates...
- The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to coordinate daily research activities in the Department of Neurology/Division of Cognitive Neurology. You will recruit, interview and enroll patients, obtain informed consent,...
- The Ohio State University in Columbus, OH seeks a Clinical Research Coordinator in Radiology to support participant-facing activities, data collection and study documentation. Responsibilities include recruiting subjects, obtaining informed consent, coordinating appointments...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Trial Manager. Be the first to apply!
- neuroscience clinical research coordinator Columbus, OH
- clinical trials manager Columbus, OH
- clinical research coordinator Columbus, OH
- clinical project manager Columbus, OH
- clinical research nurse Columbus, OH
- clinical research monitor Columbus, OH
- clinical research remote Columbus, OH
- clinical research part time Columbus, OH
- entry level clinical research Columbus, OH
- clinical trials Columbus, OH


