Clinical Research Director jobs in Norman, OK

Clinical Research Director directs and oversees the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Clinical Research Director ensures adherence to standard operating procedures, good clinical practice and FDA regulations. Requires an advanced degree. Additionally, Clinical Research Director typically reports to top management. The Clinical Research Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. To be a Clinical Research Director typically requires 5+ years of managerial experience. (Copyright 2024 Salary.com)

Recently Added Clinical Research Director jobs

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Director of Clinical Research
  • Rivus Wellness and Research Institute
  • Oklahoma, OK FULL_TIME
  • Rivus Wellness and Research Institute is growing and we are looking for individuals who are passionate about delivering exceptional patient care. In this position, you will be responsible for the overall success of the clinical research operations by managing a team of 5 individuals and providing oversite to 20 studies. Previous management experience with a track record of success is required. In general, the ideal candidate for this position will demonstrate exceptional team building skills and possess robust knowledge of Clinical Research including study conduct, regulatory compliance, HIPAA, ALCOA C, SOP creation and adherence, recruitment, contract negations, initiation of training programs, employee retention, departmental budgeting, and professionalism. Pervious experience with Central Nervous trials is preferred, but not required. 

    Essential Duties

    • Develop a team of individuals capable of conducting the site's extensive research portfolio. 
    • Collaborate with executive team regarding efficiencies and deficiencies of daily work flow. Implement changes accordingly.
    • Develops and Implements new research processes - streamlines current research processes.
    • Ensures that sponsor has been invoiced for all completed visits.
    • Work with the Director of Patient Experience to develop relationships with community physicians and other potential referral sources.
    • Seek new study opportunities.
    • Ensure site is appropriately staffed for patient load.
    • Payroll
    • Time off requests 
    • Department budgets
    • Community outreach
    • Attend Investigator Meetings with Principal Investigator- asks questions and collects pertinent study information while at investigator meeting. Completes required protocol, EDC and any additional training while at meetings.
    • Attend Site initiation visits from various drug sponsors and conduct site initiation tours.
    • Schedule and attend PSV’s 
    • Negotiate contracts between site and sponsor.
    • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
    • Quality Assurance
    • Provide QC to Senior CRC when CRC is unavailable or unable. 
    • Ensures all documents are signed/documented by Pl.
    • Ensures all source documents are complete by rater and/or coordinator and consistent with data in the EDC before patient charts are put away.
    • Ensures all data both in source documentation and EDC is accurate according to protocol.
    • After data is verified acknowledge in Realtime/CTMS.
    • Conduct random QC audits for a selection of each CRC’s visits on a monthly basis.
    • Prepare for AND participate in quality assurance audits conducted by study sponsors and federal agencies.
    • Develops and implements new front office processes - streamlines current front office processes.
    • Implement and update research and office policies and procedures.
    • Educates staff on job duties.
    • Oversee that research staff is following policy and procedures and adhering to their job duties.
    • Submit initial regulatory packet and paperwork when awarded a new study within a timely manner.
    • Assign awarded studies to appropriate study coordinator.
    • Manages and updates Standard Operating Procedures.
    • Meet with monitor during onsite visits.
    • Attend all study training, updates, and IMV’s, both in-person and virtual. 
    Requirements
    • Previous clinical research management experience (1 years) 
    • Bachelor's Degree or equivalent experience 
    • Ability to multitask 
    • Ability to follow site SOP and sponsor protocols without deviation
    • Strong verbal and written communication skills 
    • Ability to work on multiple computer platforms for patient record keeping 
    • Ability to meet and exceed goals
    • Ability to travel if/when in person investigator meetings resume
    Additional Info
    • Monday-Friday 8am-5pm 
    • Full BENEFITS after 90 days!! 
    • FULL TIME. 40 Hrs/week
    • 2 weeks PTO 
  • 14 Days Ago
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Clinical Research Nurse (RN)
  • EmVenio Research
  • Oklahoma, OK FULL_TIME
  • ABOUT EMVENIO RESEARCH:EmVenio Research delivers localized trial access to diverse and underserved communities. We empower patients and embrace communities on their terms. Our research solutions culti...
  • 10 Days Ago
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E
Clinical Research Coordinator
  • EmVenio Research
  • Oklahoma, OK FULL_TIME
  • ABOUT EMVENIO RESEARCH:EmVenio Research delivers localized trial access to diverse and underserved communities. We empower patients and embrace communities on their terms. Our research solutions culti...
  • 26 Days Ago
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Clinical Research Coordinator
  • Rivus Wellness and Research Institute
  • Oklahoma, OK FULL_TIME
  • Rivus Wellness and Research Institute is growing and we are looking for individuals who are passionate about delivering exceptional patient care. In this position, you will be responsible for the over...
  • 25 Days Ago
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A
Medical Receptionist
  • Allergy, Asthma & Clinical Research Center
  • Oklahoma, OK FULL_TIME
  • Medical receptionist needed for fast-paced medical practice. Detail oriented and ability to multitask are requirements for this position. High school diploma and medical receptionist experience requir...
  • Just Posted
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O
Multiple Sclerosis Clinical Innvestigator
  • Oklahoma Medical Research Foundation
  • Oklahoma, OK FULL_TIME
  • Overview Founded in 1946, the Oklahoma Medical Research Foundation (OMRF) is among the nation’s oldest, most respected independent, nonprofit biomedical research institutes. OMRF is dedicated to under...
  • 1 Month Ago
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0 Clinical Research Director jobs found in Norman, OK area

About Norman, Oklahoma

Norman (/ˈnɔːrmən/) is a city in the U.S. state of Oklahoma located 20 miles (32 km) south of downtown Oklahoma City. As the county seat of Cleveland County and a part of the Oklahoma City metropolitan area, its population was 110,925 at the 2010 census. Norman's estimated population of 122,843 in 2017 makes it the third-largest city in Oklahoma. Norman was settled during the Land Run of 1889, which opened the former Unassigned Lands of Indian Territory to American pioneer settlement. The city was named in honor of Abner Norman, the area's initial land surveyor, and was formally incorporated o...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Director jobs
$129,570 to $174,913
Norman, Oklahoma area prices
were up 1.2% from a year ago
View detail

What does a Clinical Research Director do?

Clinical Research Director in Killeen, TX
We are Looking for an Assistant Director for the Center for Clinical Research Education.
December 07, 2019
Clinical Research Director in Springfield, IL
During the Clinical Research Operations Forum a few weeks ago, Stephen Sonstein, Ph.D., Professor & Program Director for Clinical Research Administration at Eastern Michigan University spoke on the shift in clinical research going from a focus on regulatory compliance to a standardization of competencies for professionals working in the field.
February 06, 2020
Clinical Research Director in Olympia, WA
You might occasionally be able to enter from the administration side - for example, you could start as a study-site coordinator in the NHS or as a clinical trials administrator.
January 28, 2020