Top Clinical Research Executive jobs in the United States
Top Clinical Research Executive plans and directs all aspects of the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Top Clinical Research Executive ensures adherence to SOPs, Good Clinical Practice and FDA regulations. Requires an advanced degree. Additionally, Top Clinical Research Executive typically reports to top management. The Top Clinical Research Executive manages a departmental function within a broader corporate function. Develops major goals to support broad functional objectives. Approves policies developed within various sub-functions and departments. To be a Top Clinical Research Executive typically requires 8+ years of managerial experience. Comprehensive knowledge of the overall departmental function. (Copyright 2024 Salary.com)
Recently Added Top Clinical Research Executive jobs
Clinical Research Site Manager
- DM Clinical Research
-
Tomball, TX
FULL_TIME
-
Clinical Research Site ManagerThe Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Also To ensure study enrollment meets or exceeds Sponsors' expectations and company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES- Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
- Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
- Responsible for immediate supervision and performance of the assigned site staff under the supervision of the Site Director or Director of Site Operations.
- Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- Sponsor-provided and IRB-approved Protocol Training
- All relevant Protocol Amendments Training
- Any study-specific Manuals Training as applicable
- Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
- It is the responsibility of the Site Manager to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
- Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow-up on the action items, at their respective sites.
- Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
- Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs, and guidance documents.
- Ensuring data quality, subject retention, and compliance, timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
- Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
- Coaching, counseling, and disciplining the employees as applicable.
- To develop, coordinate, and enforce site-specific systems, policies, procedures, and productivity standards.
- Communicating and effective implementation of strategic goals from senior management to the site team.
- Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
- Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
- Being prepared for and available at all required company meetings.
- Submitting required administrative paperwork per company timelines.
- Occasionally attending out-of-town Investigator Meetings.
- Any other matters as assigned by management.
KNOWLEDGE & EXPERIENCEEducation:- Bachelor’s degree preferred
- Advanced degree preferred
Experience:- At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization.
Credentials:- Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.
Knowledge and Skills:- Solid teamwork, organizational, interpersonal, and problem-solving skills and attention to detail.
- Critical Thinking
- Active Listening
- Reading Comprehension — Understanding written sentences and paragraphs in work-related documents.
- Speaking and Writing to communicate effectively as appropriate for the needs of the audience.
- Ability to multitask, adhere to deadlines, and work both independently and cooperatively with interdisciplinary teams.
- Strong computer skills in relevant software and related clinical systems are required.
- Comprehensive knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs.
- 11 Days Ago
Clinical Research Assistant
- Velocity Clinical Research, Inc.
-
Meridian, ID
FULL_TIME
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
- 11 Days Ago
Clinical Research Assistant
- Velocity Clinical Research, Inc.
-
Cincinnati, OH
PER_DIEM
- Overview Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we ...
- 11 Days Ago
Clinical Research Nurse
- Alcanza Clinical Research
-
Clermont, FL
FULL_TIME
- Clinical Research NurseDepartment: Operations Employment Type: Full TimeLocation: Vertex Clinical Research | Clermont FLReporting To: Austin WingDescriptionAlcanza is a growing multi-site, multi-phase...
- 14 Days Ago
Top Clinical Research Executive jobs at Popular Companies
Clinical Research Coordinator (Research Professional 1)
- University Of Minnesota
-
Minneapolis, MN
- About the Job We are seeking a Clinical Research Coordinator (Research Professional 1) in the Interventional Psychiatry ...
- 4/19/2024 12:00:00 AM
Senior Research Executive
- Laslo Fox
-
- We are seeking a highly skilled Quantitative Senior Research Executive to join a successful Pharmaceutical Research Cons...
- 4/18/2024 12:00:00 AM
Researcher - Executive Search
- FIFTEEN WEST
-
- ROLE: Associate Consultant - Executive Search LOCATION: New York, Midtown CLIENT: Boutique Global Executive Search firm ...
- 4/18/2024 12:00:00 AM
Senior Research Executive (Quantitative)
- Branding Science Group
-
Princeton, NJ
- Senior Research Executive (Quantitative) Location: Hybrid working (New Jersey/home-based) Salary: $75,000 - $80,000 per ...
- 4/18/2024 12:00:00 AM
DERMS and Microgrid Researcher Staff IV
- Electric Power Research Institute, Inc.
-
Knoxville, TN
- Job Title: DERMS and Microgrid Researcher Staff IV Location: Knoxville, TN Job Summary and Description: Job Description ...
- 4/18/2024 12:00:00 AM
Senior Research Executive (Quantitative)
- PERMEVO
-
Princeton, NJ
- JOB TITLE: Senior Research Executive (Quantitative) LOCATION: Princeton, NJ TYPE: (Hybrid working: New Jersey/home-based...
- 4/17/2024 12:00:00 AM
Unpaid Clinical Research Team Member/Intern
- AVIATI HEALTHCARE LLC
-
Memphis, TN
- Job Description Job Description Looking for an opportunity to experience clinical research at the site level. The respon...
- 4/16/2024 12:00:00 AM
Research Coordinator (Research Professional 2)
- University of Minnesota
-
Minneapolis, MN
- About the Job This full-time research coordinator position will join a dynamic research laboratory using cutting edge re...
- 4/15/2024 12:00:00 AM
Income Estimation for Top Clinical Research Executive jobs
$210,619 to $384,389