139 Clinical Research Assistant (Medical Assistant) Jobs in San Antonio, TX
Pinnacle Clinical Research, LLC is Hiring a Clinical Research Assistant (Medical Assistant) Near San Antonio, TX
- 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
- 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
- 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
- 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 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.
- 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!
Job Summary
Full Time
$65k-86k (estimate)
04/11/2024
06/10/2024
pinnacleresearch.com
HOUSTON, TX
<25
2016
NAWAB F BALOCH
<$5M
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About Pinnacle Clinical Research, LLC
Pinnacle Clinical Research is dedicated to conducting late phase clinical trials in the areas of Hepatology and Gastroenterology, with a special focus on fatty liver disease. We pride ourselves on conducting high quality research as a complement to the medical care that our volunteers receive from their routine care center.
The job skills required for Clinical Research Assistant (Medical Assistant) include Clinical Research, Clinical Trial, Problem Solving, Patient Care, Coordination, Initiative, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Assistant (Medical Assistant). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Assistant (Medical Assistant). Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Research Assistant (Medical Assistant) positions, which can be used as a reference in future career path planning. As a Clinical Research Assistant (Medical Assistant), it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Assistant (Medical Assistant). You can explore the career advancement for a Clinical Research Assistant (Medical Assistant) below and select your interested title to get hiring information.
If you are interested in becoming a Clinical Research Assistant, you need to understand the job requirements and the detailed related responsibilities. Of course, a good educational background and an applicable major will also help in job hunting. Below are some tips on how to become a Clinical Research Assistant for your reference.
Step 1: Understand the job description and responsibilities of an Accountant.
Quotes from people on Clinical Research Assistant job description and responsibilities
Certifications are also available for this position through The Society of Clinical Research Associates (SOCRA) and The Association of Clinical Research Professionals.
01/04/2022: Santa Barbara, CA
Analyze and evaluate clinical data gathered during research.
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Provide regular report updates of the progress of clinical studies to the appropriate personnel.
03/23/2022: Santa Cruz, CA
These clinical trials are very much regulated and seriously monitored to ensure that they comply with the laid down regulations.
01/04/2022: Frankfort, KY
Must be able to ensure that data gotten from clinical trials are accurate and reliable and the legal rights and privacy of the subjects are protected.
02/02/2022: Racine, WI
Step 2: Knowing the best tips for becoming an Accountant can help you explore the needs of the position and prepare for the job-related knowledge well ahead of time.
Career tips from people on Clinical Research Assistant jobs
Fact-checking, editing, and proofreading research documents for accuracy and consistency.
01/16/2022: Green Bay, WI
Research Assistants provide support to research teams who are conducting experiments or gathering and analysing data.
03/14/2022: Provo, UT
Maintained FDA clinical trial documentation for department and received excellent FDA audits of records.
03/02/2022: Fort Wayne, IN
Have strong customer focus and good communication skills
02/11/2022: Milwaukee, WI
For example, clinical research associate candidates should have excellent attention to detail and organizational skills since they’re responsible for monitoring and reporting on the results of clinical trials.
12/27/2021: Everett, WA
Step 3: View the best colleges and universities for Clinical Research Assistant.
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