Clinical Research Manager jobs in Brownsville, TX
Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Clinical Research Manager jobs
Research Assistant (Medical Assistant)
- Pinnacle Clinical Research, LLC
-
Brownsville, TX
FULL_TIME
-
Come join our team and make a difference as we blaze the way into the future of liver medicine. Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatty liver disease (non-alcoholic). We pride ourselves on conducting high quality research as a complement to the medical care that our volunteers receive from their routine care center. Be a part of the discovery!Summary: Pinnacle Clinical Research seeks a Clinical Research Assistant, responsible for assisting with the day-to-day operations of clinical trials alongside the Clinical Research Coordinator and Investigators, assisting in project planning, and ensuring that pre-established work scope, study protocol, and regulatory requirements are followed. They will attend meetings and events to promote studies, recruit, and pre-screen study participants. This person must be able to understand clinical trial priorities and establish a workflow to complete all required activities in a timely manner. This position is responsible for a broad range of duties involving confidential information.The Clinical Research Assistant must be organized, excel at multi-tasking, detail-oriented, an excellent communicator, and be able to provide high quality patient care. This person will collaborate very closely with other members of the PCR team, external vendors, and therefore must be highly collaborative, goal-oriented, flexible, and communicative. An ideal candidate will be responsive, thoughtful, empathetic, initiative-taking, and a team-player. This role reports directly to the Clinical Research Project Manager.Duties and Responsibilities:Clinical Trial Execution:
- Exercise judgement within the allowable limits defined within clinical trial protocols, standard operating procedures, and the direction from the Clinical Research Coordinators (CRC), study investigator, Project Manager, and Director of Clinical Research Operations
- Always maintain subject and document confidentiality, understand, and comply with the appropriate sponsor requirements and regulations which include the Food and Drug Administration, good clinical practices, International Conference on Harmonization, Health Insurance Portability and Accountability Act, institutional review boards, and institutional policies and procedures
- Complete study directed assessments with patients which include, but not limited to, subject history, adverse events, Fibroscan, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessment
- Assist and complete study related documents and new study preparation
- Function as a secondary liaison with pharmaceutical sponsors and external vendors
- Respond to internal and external requests for information in a timely manner
- Perform subject pre-screening and recruitment
- Contribute to data management for research projects
- Identify opportunities to improve patient care and satisfaction
- Conduct patient-facing encounters with compassion, empathy, and thoroughness
- Perform laboratory and/or pharmacy duties as outlined in the protocols and/or manuals as directed
- Assists with the preparation for study monitor visits and/or audits as directed
- Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients
Administration:- Complete electronic case report forms
- Create and maintain reports and/or spreadsheets as requested
- Enter all patient data into the clinical trial management system in a timely manner
- Assist with maintaining study documents and electronic regulatory documents
- Organize and file study documents in regulatory binders
- Request medical records and maintain the applicable spreadsheet(s)
- Assist with organizing study inventory (IP, Lab Kits, etc.)
- Assist with data entry in study assigned portals as applicable
- Assists with coordinating multiple projects with competing priorities and deadlines, as needed based on clinical trial protocol directives and study volume
Duties, responsibilities, and activities may change, or new ones may be assigned at any time.Qualifications:- High school diploma or general education degree (GED) required
- Associate or bachelor’s Degree in scientific area of study or equivalent combination of education, training, and experience preferred
- Proficient in all Microsoft Office applications
- Proficient in Clinical Research IO (CRIO) or equivalent CTMS preferred, but training will be provided during onboarding
- Must have strong knowledge of ICH/GCP guidelines
- Must complete CITI and GCP training before interacting with participants and must re-certify every 3 years
- Must be trained and certified in administration of Fibroscan, training provided during onboarding
- Must have basic life support (BLS) training, provided during onboarding
- Valid driver's license with maintenance of safe driving record and an automobile that is insured in accordance with the state
- Demonstrated organizational skills and outstanding time management, including keen attention to detail with the ability to track multiple projects at one time
- Strong written and oral communication skills
- Knowledge of basic medical terminology
- Possess impeccable integrity and personal and professional values that are consistent with PCR’s high standards and mission
- Comply with the company policies, code of ethics, and guiding values always
- Proficient in English and Spanish preferred
Competencies:- Must be able to effectively communicate with all levels of internal and external contacts
- Ability to work independently and multi-task in a fast-paced team environment
- Strong people skills including ability to interact with individuals from diverse backgrounds and to oversee confidential matters and sensitive information with discretion and judgment
- Must possess a positive, friendly, and professional demeanor, particularly when interacting with patients
- Must be able to work independently and collaborate with a team
- Ability to interpret clinical research protocols
- Strong problem-solving and decision-making skills, particularly when under pressure
- Proactive at identifying, addressing, and solving issues in real time
- Energetic self-starter, results oriented, and the ability to work effectively in an entrepreneurial environment
Work Environment and Physical demands:The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.- Work is performed in an office/laboratory and/or a clinical environment.
- Exposure to biological fluids and/or bloodborne pathogens.
- Personal protective equipment required such as protective eyewear, garments, and gloves.
- Occasional travel may be required domestic and/or international.
- Ability to work in an upright and/or stationary position for 6-10 hours per day.
- Frequent mobility required.
- Occasionally squatting, kneeling, or bending.
- Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.
Benefits of working at Pinnacle Clinical Research:- 401k
- Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
- 3 weeks of paid time off
- Twelve paid company holidays
- Tranquility Room
- Pinnacle Gym
- Scrub voucher (specific positions apply)
- And more!
Pinnacle Clinical Research is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved. - 15 Days Ago
Front Desk Scheduler
- Pinnacle Clinical Research, LLC
-
Brownsville, TX
FULL_TIME
- Come join our team and make a difference as we blaze the way into the future of liver medicine. Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatt...
- 16 Days Ago
Sub Investigator
- Pinnacle Clinical Research, LLC
-
Brownsville, TX
FULL_TIME
- Come join our team and make a difference as we blaze the way into the future of liver medicine. Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatt...
- 16 Days Ago
Sub Investigator (FT)
- Pinnacle Clinical Research, LLC
-
Brownsville, TX
FULL_TIME
- Come join our team and make a difference as we blaze the way into the future of liver medicine. Pinnacle Clinical Research is dedicated to conducting cutting-edge research with a special focus on fatt...
- 15 Days Ago
Travel Nurse - RN - Clinical Research
- PCM Trials
-
Brownsville, TX
FULL_TIME
- Travel Nurse - RN - Clinical Research Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing per diem/PRN position for PCM Trials. A PCM ...
- 9 Days Ago
Pharmaceutical Sales Representative
- Syneos Health Clinical
-
Brownsville, TX
FULL_TIME
- Description You have what it takes: a competitive drive coupled with exceptional sales ability. In this role, you will be an integral part of a nationwide sales team developing and managing an assigne...
- 7 Days Ago
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0 Clinical Research Manager jobs found in Brownsville, TX area
Principal Scientist
- Bausch + Lomb
-
Harlingen, TX
- Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
- 4/26/2024 12:00:00 AM
Principal Scientist
- Bausch + Lomb
-
Harlingen, TX
- Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
- 4/26/2024 12:00:00 AM
Research Assistant_Informatics & Engineering Systems
- University of Texas Rio Grande Valley
-
Brownsville, TX
- Title Information Assistantship TitleResearch Assistant_Informatics & Engineering Systems Job Class Code00095 FLSAExempt...
- 4/25/2024 12:00:00 AM
Travel Cath Lab Technologist - $2,603 per week
- Stability Healthcare
-
Harlingen, TX
- Epic Travel Staffing Allied is seeking a travel Cath Lab Technologist for a travel job in Harlingen, Texas. Job Descript...
- 4/25/2024 12:00:00 AM
Travel Cath Lab Technologist - $3,280 per week
- Hiring Now!
-
Harlingen, TX
- A Best Placement Services is seeking a travel Cath Lab Technologist for a travel job in Harlingen, Texas. Job Descriptio...
- 4/25/2024 12:00:00 AM
Senior Scientist
- Bausch + Lomb
-
Brownsville, TX
- Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
- 4/24/2024 12:00:00 AM
Practice Director- Brownsville, Tx
- Us Oncology Network-wide Career Opportunities
-
Brownsville, TX
- OverviewTexas Oncology is looking for a Practice Director to join our team ! This position will support and lead all the...
- 4/23/2024 12:00:00 AM
Echo Technician - $25-36 per hour
- Hiring Now!
-
Harlingen, TX
- Baptist Health System - San Antonio TX is seeking a Echo Technician for a job in Harlingen, Texas. Job Description & Req...
- 4/23/2024 12:00:00 AM
About Brownsville, Texas
Brownsville is one of the southernmost cities in the contiguous United States; only a handful of municipalities in Florida's Miami-Dade and Monroe counties (plus Everglades City in Collier County) are located farther south than Brownsville. The city has a total area of 84.867 square miles (219.805 km2), of which 81.528 square miles (211.157 km2) of it is land and 3.339 square miles (8.648 km2) is water, according to the United States Census Bureau of 2017.
The city is situated at the intersection of different climates (subtropical, Chihuahuan Desert, Gulf Coast plain, and Great Plains); this p...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$85,538 to $113,332
Brownsville, Texas area prices
were up 1.2% from a year ago
were up 1.2% from a year ago
What does a Clinical Research Manager do?
Clinical Research Manager in Springfield, IL
Generally, employers are looking for Clinical Research Managers who have a Bachelors degree.
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Clinical Research Manager in Colorado Springs, CO
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Clinical Research Manager in Little Rock, AR
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January 12, 2020