Scientist - Clinical Research jobs in Pasadena, TX
Scientist - Clinical Research assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Being a Scientist - Clinical Research secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Additionally, Scientist - Clinical Research interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. The Scientist - Clinical Research work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Scientist - Clinical Research typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)
Recently Added Scientist - Clinical Research 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.
- 14 Days Ago
Clinical Research Regulatory Assistant
- DM Clinical Research
-
Tomball, TX
FULL_TIME
- Clinical Research Regulatory AssistantLocationTomballEmployment TypeFull-TimeMinimum ExperienceEntry-levelDM Clinical Research, in partnership with the Texas Center for Drug Development, is looking fo...
- 19 Days Ago
Clinical Research Rater
- DM Clinical Research
-
Bellaire, TX
PART_TIME
- Clinical Research Rater The Clinical Research Rater is responsible for conducting neurocognitive test evaluations and interviews/ratings on study participants according to the study protocol. They pla...
- 4 Days Ago
Clinical Research Regulatory Specialist
- DM Clinical Research
-
Tomball, TX
FULL_TIME
- Clinical Research Regulatory SpecialistDepartmentTomballEmployment TypeFull-TimeMinimum ExperienceExperiencedDM Clinical Research, the largest privately-owned research management organization in the H...
- 4 Days Ago
Clinical Research Regulatory Specialist
- DM Clinical Research
-
Tomball, TX
FULL_TIME
- Clinical Research Regulatory SpecialistDepartmentTomballEmployment TypeFull-TimeMinimum ExperienceExperiencedDM Clinical Research, the largest privately-owned research management organization in the H...
- 4 Days Ago
Clinical Research Site Manager
- DM Clinical Research
-
Humble, TX
FULL_TIME
- Clinical Research Site ManagerDepartmentClinical Operations - HumbleEmployment TypeFull-TimeMinimum ExperienceSenior Manager/SupervisorDM Clinical Research, the largest privately-owned research manage...
- 6 Days Ago
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0 Scientist - Clinical Research jobs found in Pasadena, TX area
Data Scientist
- Brooksource
-
Houston, TX
- Title: Data Scientist Company: Brooksource Fortune 500 Client Contract Period: 3-months Contract: Contract-to-Hire Sched...
- 4/22/2024 12:00:00 AM
Scientist/Senior Scientist (Embryologist)
- Commonwealth Sciences Inc.
-
Houston, TX
- Position located in Fort Worth, TXResponsibilities of the Scientist/Senior Scientist (Embryologist):Will perform Somatic...
- 4/22/2024 12:00:00 AM
Data Scientist
- Brooksource
-
Houston, TX
- Title: Data Scientist Company: Brooksource Fortune 500 Client Contract Period: 3-months Contract: Contract-to-Hire Sched...
- 4/22/2024 12:00:00 AM
Data Scientist
- Strategic Staffing Solutions
-
Houston, TX
- Strategic Staffing Solutions is looking for a Data Scientist in Houston, TX.We are currently seeking a forward-thinking ...
- 4/22/2024 12:00:00 AM
Lead Data Scientist
- The Friedkin Group
-
Houston, TX
- LIVING OUR VALUES All associates are guided by Our Values. Our Values are the unifying foundation of our companies. We s...
- 4/22/2024 12:00:00 AM
Environmental Scientist
- Hire Resolve
-
Katy, TX
- Job Description Job Description Hire Resolves client is a leading Environmental Services that is urgently seeking the ex...
- 4/22/2024 12:00:00 AM
Data Scientist
- X4 Technology
-
Houston, TX
- Company & Role: This is a fantastic opportunity to join an internationally renowned Energy company where you will get to...
- 4/20/2024 12:00:00 AM
Senior Scientist
- Bausch + Lomb
-
Houston, TX
- Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
- 4/20/2024 12:00:00 AM
About Pasadena, Texas
Pasadena /ˌpæsəˈdiːnə/ is a city in the U.S. state of Texas, within the Houston–The Woodlands–Sugar Land metropolitan area. As of the 2010 U.S. Census, the city's population is 149,043, making it the seventeenth most populous city in the state of Texas, as well as the second-largest city in Harris County. The area was founded in 1893 by John H. Burnett of Galveston, who named the area after Pasadena, California, because of the perceived lush vegetation.
The Pasadena Volunteer Fire Department is the largest of all volunteer municipal fire departments in the United States.
According to the Unite...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Scientist - Clinical Research jobs
$83,411 to $118,592
Pasadena, Texas area prices
were up 2.3% from a year ago
were up 2.3% from a year ago
What does a Scientist - Clinical Research do?
Scientist - Clinical Research in El Paso, TX
DDCF's Medical Research Program created the Clinical Scientist Development Award to provide mentored research funding to early-career physician-scientist faculty to enable their transition to independent and successful research careers.
December 01, 2019
Scientist - Clinical Research in Green Bay, WI
Jude Children’s Research Hospital, talented faculty and staff work together and with colleagues worldwide-to advance the resear.
January 26, 2020
Scientist - Clinical Research in Sacramento, CA
Bachelor s in Life Sciences or related field with 2 plus years of clinical research experience.
January 11, 2020