Current jobs related to Senior Clinical Research Coordinator - Columbus - OhioHealth
-
Clinical Research Coordinator
1 week ago
Columbus, United States OPTIMED RESEARCH LTD Full timeSummary: The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily...
-
Clinical Research Coordinator
2 weeks ago
Columbus, United States OPTIMED RESEARCH LTD Full time $45,000 - $70,000Job DescriptionJob Description Summary: The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports,...
-
Clinical Research Coordinator
2 weeks ago
Columbus, United States OPTIMED RESEARCH LTD Full time $45,000 - $70,000Job DescriptionJob DescriptionSummary:The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates...
-
Senior Clinical Research Coordinator
2 months ago
Columbus, Ohio, United States Ohio Health Full timeWe are more than a health system. We are a belief system. We believe wellness and sickness are both part of a lifelong partnership, and that everyone could use an expert guide. We work hard, care deeply and reach further to help people uncover their own power to be healthy. We inspire hope. We learn, grow, and achieve more - in our careers and in our...
-
Clinical Research Coordinator I
1 month ago
Columbus, Ohio, United States Nationwide Children's Hospital Full timeOverview We are seeking a part-time Clinical Research Coordinator to join Principal Investigator Dr Sarah O'Brien's research laboratory. Delayed diagnosis of bleeding disorders in women is an important public health issue. Dr O'Brien's research focuses on the intersections between women's health and hematology and seeks to improve recognition of bleeding...
-
Clinical Research Nurse Coordinator
6 hours ago
Columbus, Ohio, United States Nationwide Children's Hospital Full timeAbout the RoleWe are seeking a highly skilled and dedicated Clinical Research Coordinator RN to join our team at Nationwide Children's Hospital. As a key member of our research team, you will play a critical role in ensuring the successful execution of clinical trials and providing exceptional patient care.Key ResponsibilitiesPlan, implement, and evaluate...
-
Clinical Research Coordinator I
10 hours ago
Columbus, Ohio, United States Nationwide Children's Hospital Full timeJob SummaryWe are seeking a highly skilled Clinical Research Coordinator I to join our team at Nationwide Children's Hospital. The successful candidate will be responsible for managing key elements of clinical research studies to meet protocol obligations.Key ResponsibilitiesConduct clinical research studies as outlined in the study protocol, ensuring...
-
Research Coordinator
2 weeks ago
Columbus, United States Ohio Gastroenterology Group Inc Full timeJob DescriptionJob DescriptionJob Objective: The Research Coordinator will facilitate all facets of GI clinical research studies.Duties and Responsibilities:· ·Administratively and clinically manage industry sponsored clinical trials· Assist with protocol design, where requested· Adhere to Research SOP’s, Good Clinical Practices and the study...
-
Clinical Research Nurse
2 days ago
Columbus, United States Ohio State University Wexner Medical Center Full timeClinical Research Nurse (CRN) to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Weafer Alcohol Research Laboratory in the Department of Psychiatry and Behavioral Health. We are an advanced cognitive neuroscience research lab studying alcohol use, with a focus on sex differences and risk...
-
Clinical Research Nurse
2 weeks ago
Columbus, United States Ohio State University Wexner Medical Center Full timeClinical Research Nurse (CRN) to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Weafer Alcohol Research Laboratory in the Department of Psychiatry and Behavioral Health. We are an advanced cognitive neuroscience research lab studying alcohol use, with a focus on sex differences and risk...
-
Clinical Research Nurse
4 weeks ago
Columbus, United States Ohio State University Wexner Medical Center Full timeClinical Research Nurse in the area of Benign Hematology in the Division of Hematology within the Department of Internal Medicine; plans; organizes and coordinates care of patients in benign hematology protocols; performs clinical duties and other tasks associated with clinical research trials including patient care, data entry and recruitment of...
-
Clinical Research Nurse Specialist
3 hours ago
Columbus, Ohio, United States Ohio State University Wexner Medical Center Full timeJob SummaryWe are seeking a highly skilled and organized Clinical Research Nurse to join our team at the Ohio State University Wexner Medical Center. The successful candidate will be responsible for coordinating and performing daily clinical research activities in accordance with approved protocols.Key ResponsibilitiesCoordinate and manage clinical aspects...
-
Researcher Senior Associate
3 months ago
Columbus, United States InsideHigherEd Full timeScreen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.Current Employees and Students:If you are currently employed or enrolled as a student at The Ohio State University,...
-
Research Compliance Coordinator
1 week ago
Columbus, Ohio, United States The Ohio State University Full timeCurrent Employees and Students If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to explore available positions. To ensure your application is complete, please follow these steps: ...
-
Clinical Research Nurse
1 month ago
Columbus, United States Ohio State University Wexner Medical Center Full timeClinical Research Nurse to organize and coordinate care of patients on clinical research protocols in Comprehensive Cancer Center to include evaluation of patient eligibility and registration of out/in patients, monitors care and ensures proper follow up. Responsibilities Evaluates patient response and complications Develops and revises patient care...
-
Clinical Research Associate
1 week ago
Columbus, Ohio, United States InsideHigherEd Full timePosition Title: Junior Research ScientistDepartment: Medicine | Surgical OncologyA dedicated Research Associate is sought to contribute to a pioneering research facility. This role encompasses the planning, design, and oversight of research initiatives with a primary focus on pancreatic cancer. Key responsibilities include:Collecting and processing...
-
Clinical Lab Research Coordinator
3 days ago
Columbus, Ohio, United States Nationwide Children's Hospital Full timeJob SummaryThe Clinical Lab Research Coordinator will collaborate with senior leadership to maintain technical and procedural operations in the laboratory section. This role will assist in project development, quality assurance, training, and competency testing for staff.Key ResponsibilitiesDevelop and implement new or improved procedures and...
-
Research Compliance Coordinator
3 days ago
Columbus, Ohio, United States The Ohio State University Full timeCurrent Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to explore positions of interest. To ensure your application is complete, please follow these steps: Gather all...
-
Research Compliance Coordinator
3 days ago
Columbus, Ohio, United States The Ohio State University Full timeCurrent Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to explore available positions of interest. To ensure your application is thorough, please follow these steps:...
-
Research Compliance Coordinator
3 days ago
Columbus, Ohio, United States The Ohio State University Full timeCurrent Employees and Students If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to explore available positions that align with your interests. To ensure your application is thorough, please...
![OhioHealth](https://media.trabajo.org/img/noimg.jpg)
Senior Clinical Research Coordinator
1 month ago
We are more than a health system. We are a belief system. We believe wellness and sickness are both part of a lifelong partnership, and that everyone could use an expert guide. We work hard, care deeply and reach further to help people uncover their own power to be healthy. We inspire hope. We learn, grow, and achieve more – in our careers and in our communities.
Job Description Summary:
The Senior Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. This position performs day to day activities related to clinical research studies including: recruit and screen participants, obtains informed consent, educate participants regarding study requirements, event reporting and complete case report forms. This position performs activities independently, consistently and accurately and demonstrates skills and abilities resulting in high quality work. This position applies these skills to a broad range of different type of clinical studies, navigates available resources appropriately, effectively uses all tools at their disposal and operates e-technology proficiently. The Senior Clinical Consultant Research performs the majority of activities independently and performs quality checks of their work. This position serves as a formal and informal leader of multidisciplinary teams establishing and maintaining communications with Investigator, research team, sponsor, and other applicable individuals/groups.Minimum Qualifications:
Bachelor's Degree (Required)- Degree required from a four year college or university
- Two years of direct human subjects research
- Two years of direct clinical research experience
SPECIALIZED KNOWLEDGE
- Applies critical thinking and creative problem solving skills across a wide variety of clinical studies
- Ability to prioritize the work of multiple projects.
- Experience in a team setting.
- Strong verbal and written communication skills, as well as customer service skills and ability to problem solve, prioritize and manage multiple tasks
- Strong computer skills, including thorough knowledge of systems (EMR, Microsoft)
DESIRED ATTRIBUTES
- Clinical Research Coordinator Certification (or equivalent approved Clinical Research Certification)
- Three or more years of direct human subjects research
- Clinical knowledge in assigned therapeutic area or program
MAJOR DUTIES/RESPONSIBILITIES & ESSENTIAL FUNCTIONS
Study Planning and Coordination
Implements the requirements of clinical research protocols in compliance with local, state, institutional, Federal (FDA, DHHS) and sponsor requirements.
Accountable to PI for study specific responsibilities and functions with assistance on multiple clinical research studies.
Works closely with PI to organize, plan and carryout the research in an efficient and timely manner.
Assists with protocol feasibility, resource requirements and study panning activities including leading internal training to implement the protocol and avoid deviations.
Develop and plan recruitment procedures for potential participants and oversee the enrollment of the clinical trial as directed by the PI.
Ensures that study parameters are correctly applied prior to a research participant enrolling a study and during the research participant’s visits and assessments.
Extracts and records physical findings, laboratory data and other details essential to each study onto the required data collection forms accurately and within the designated time period
Attends investigator’s meetings, pre-study site visits which may require travel, study initiation visits, and all other study-related visits by monitors or Sponsor representatives.
As needed, organize and/or participate in-house protocol meetings to review study-related procedures, staffing and visit flow.
Participates in the ongoing Informed Consent process with the Investigator to ensure that research participants and their families (if applicable) have their questions answered and understand the consent form, as well as participant’s responsibilities in the study.
Responsible for giving participant instructions and serves as the primary contact for subjects by being available to handle study specific questions, concerns or events.
Accurately records and extracts data from source documentation onto report forms (paper or electronic) in a timely manner. Maintains accurate and timely source documentation.
After closeout visits have been conducted, prepares study documents for archiving according to timelines.
Responsible for in-depth knowledge of protocol requirements and GCP guidelines.
Performs other related duties as assigned or required.
Patient Care
Works with nursing and clinical staff and applies skills and knowledge to facilitate the care of research participants.
Works with nursing and clinical staff and utilizes knowledge of disease processes to observe and report adverse events and protocol violations / deviations in a timely and accurate manner to the Investigator to ensure the health, safety and welfare of the participant.
Quality and Compliance
Assume responsibility for audit preparedness activities for OHRI.
Oversees the preparation of records for periodic audits by sponsors, CROs, regulatory agencies, and internal reviews.
Assists with monitoring visits on site and is available during visits for corrections, questions, etc.
Maintains study records according to sponsor and/or regulations.
Keep records in a secure location.
Reporting
Assist in the development of reporting metrics.
Generates reports and reviews to ensure validity of data.
Provide ad hoc reports.
Communication
Demonstrates effective communications and leadership skills.
Communicates information in a timely and accurate manner with minimal supervision.
Functions as a liaison with sponsor and investigator regarding the preparation, execution and completion of studies.
Adapts communication skills in response to various situations including those related to differences in culture, age, education and other communication barriers.
Uses various media forms to maximize communication success.
Demonstrates teamwork characteristics.
Ability to manage time, prioritize and follow up on projects as necessary taking into consideration the need for flexibility when working on multiple projects.
Participates in meetings with OHRI, PI and clinical teams to review patient status at a detailed level.
Develops strategies and recommends initiatives / improvements to Manager, Research to meet the needs of OHRI and using resources wisely to achieve maximum results.
Oversee and monitor tasks which impact a process or policy change for the department.
Work with research staff to effectively communicate patient process for each trial for the life of the study.
Advise, communicate and reinforce standard practices, regulations to following regarding research study participation.
Mentorship of the clinical research process to the junior clinical research staff.
Role models best practices and fosters leadership development with the team.
Other
Attends relevant training courses on policy and compliance.
Ensures assigned training is complete and meets internal qualifications.
Responsible for completing all necessary training for their position.
Maintain familiarity with evolving regulatory and compliance context.
Other duties as assigned.
Work Shift:
DayScheduled Weekly Hours :
40Department
Oncology Research Clinical ServicesJoin us
... if your passion is to work in a caring environment
... if you believe that learning is a life-long process
... if you strive for excellence and want to be among the best in the healthcare industry
Equal Employment Opportunity
OhioHealth is an equal opportunity employer and fully supports and maintains compliance with all state, federal, and local regulations. OhioHealth does not discriminate against associates or applicants because of race, color, genetic information, religion, sex, sexual orientation, gender identity or expression, age, ancestry, national origin, veteran status, military status, pregnancy, disability, marital status, familial status, or other characteristics protected by law. Equal employment is extended to all person in all aspects of the associate-employer relationship including recruitment, hiring, training, promotion, transfer, compensation, discipline, reduction in staff, termination, assignment of benefits, and any other term or condition of employment
Discover your purpose and passion at OhioHealth
Our associates are the reason for our strength and success. Every day, they help fulfill our mission to provide exceptional care for all — with support and recognition at every turn. Apply to make a difference not only in our patient’s lives, but in yours as well.
The nursing career you always dreamed of
Nurses at all of our OhioHealth facilities have opportunities to apply and advance their skills. With support from central Ohio’s largest health system and an environment that fosters innovation and collaboration, can provide quality care for patients in the areas that mean most to you.
You choose your own pathEvery day presents something exciting and different for our nurses. As your nursing interests grow, change and advance, our established programs can help you transition to the area of care that’s most aligned with your career goals.
Every nurse has a powerful voice hereAn empowered nurse is the most impactful and satisfied nurse. Our collaborative environment ensures your ideas are heard, your opinions are respected and your initiative is rewarded. This welcoming, open-minded environment has helped earn us recognition as a three-MAGNET system.