Clinical Research Coordinator jobs in San Antonio, TX
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
Clinical Research Assistant (Medical Assistant)
- Pinnacle Clinical Research
-
San Antonio, 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. - 12 Days Ago
Senior Clinical Research Associate
- OnPoint Clinical Staffing Services
-
San Antonio, TX
FULL_TIME
- Job DescriptionSenior CRAResponsibilities include:* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical t...
- 1 Month Ago
Clinical Research Nurse, FT Nights
- EVOLUTION RESEARCH GROUP
-
San Antonio, TX
OTHER
- Job Details Job Location: LOC004 ECT Endeavor Clinical Trials LLC - San Antonio, TX Salary Range: Undisclosed Clinical Research Nurse (FT)Title: Registered Nurse (RN) - FT nights Location: San Antonio...
- 10 Days Ago
Clinical Research Assistant
- Foundation for Advancing Veterans' Health Research (FAVHR)
-
San Antonio, TX
FULL_TIME
- SUMMARY This position provides specialized administrative support in a clinical research environment. This includes pre and post award activities and regular communications/meetings with faculty and s...
- 29 Days Ago
Site Intelligence Liaison
- Summit Clinical Research Llc
-
San Antonio, TX
FULL_TIME
- Overall responsibility Responsible for completing a wide range of administrative and support activities for the Medical Science Liaison to facilitate the efficient operations of the department by perf...
- 15 Days Ago
PROMOTORA DE SALUD (Part-Time)
- Pinnacle Clinical Research, LLC
-
San Antonio, TX
PART_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
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0 Clinical Research Coordinator jobs found in San Antonio, TX area
Clinical Research Coordinator
- SQRL
-
San Antonio, TX
- Opportunity to join a prestigious clinical research site in San Antonio focused on advancing treatment options in women'...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator (CRC)
- Synergyst Research Group/Discovery Clinical Trials
-
San Antonio, TX
- Job Description Job Description (SALARY WILL BE BASED ON YOUR EXPERIENCE) Job description Responsibilities: - Coordinate...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator I
- Flourish Research
-
San Antonio, TX
- Job Description Job Description Flourish Research is looking for motivated, talented, creative individuals who want to l...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator
- Sqrl
-
San Antonio, TX
- Opportunity to join a prestigious clinical research site in San Antonio focused on advancing treatment options in women'...
- 4/23/2024 12:00:00 AM
Clinical Research Coordinator (CRC)
- SQRL
-
San Antonio, TX
- Job Description Job Description Opportunity to join a prestigious clinical research site in San Antonio focused on advan...
- 4/22/2024 12:00:00 AM
Clinical Research Assistant
- Sqrl
-
San Antonio, TX
- Opportunity to join a prestigious clinical research site in San Antonio focused on advancing treatment options in women'...
- 4/22/2024 12:00:00 AM
Travel Clinical Research Coordinator, US Based (San Antonio, TX)
- Care Access
-
San Antonio, TX
- What We Do Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks dow...
- 4/20/2024 12:00:00 AM
Clinical Research Assistant
- SQRL
-
San Antonio, TX
- Opportunity to join a prestigious clinical research site in San Antonio focused on advancing treatment options in women'...
- 4/20/2024 12:00:00 AM
About San Antonio, Texas
San Antonio (/ˌsæn ænˈtoʊnioʊ/; from Spanish, "Saint Anthony"), officially the City of San Antonio, is the seventh-most populous city in the United States, and the second-most populous city in both Texas and the Southern United States, with more than 1.5 million residents. Founded as a Spanish mission and colonial outpost in 1718, the city became the first chartered civil settlement in present-day Texas in 1731. The area was still part of the Spanish Empire, and later of the Mexican Republic. Today it is the state's oldest municipality.
The city's deep history is contrasted with its rapid rec...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$56,838 to $76,639
San Antonio, Texas area prices
were up 1.2% from a year ago
were up 1.2% from a year ago
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Monterey, CA
Coordinators often become the front line for patients because they feel more comfortable with us.
November 07, 2019
Clinical Research Coordinator in Bakersfield, CA
If you have a medical experience you may need a certificate program to work as a CRC bt if there is none then you will need an education program that covers all the required medical and research coursework in clinical research.
October 27, 2019
Clinical Research Coordinator in New Bedford, MA
If you’re looking for a job you can complete at home that lets you use your organizational and leadership skills, a career in clinical research coordination could be for you.
October 09, 2019