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Job Description:
We are seeking a motivated and detail-oriented Clinical Research Assistant to join our dynamic research team. The successful candidate will play a pivotal role in supporting clinical trials and research studies aimed at advancing medical knowledge and improving patient care. The Clinical Research Assistant will work closely with the research team, study participants, and healthcare professionals to ensure the smooth and ethical execution of research projects.
Key Responsibilities:
Participant Recruitment and Screening:Identify and recruit eligible study participants according to study criteria.
Screen potential participants to ensure their suitability for the research.
Data Collection and Documentation:Assist in the collection of clinical data, including medical histories, laboratory results, and vital signs.
Maintain accurate and organized records of all research-related activities.
Ensure data integrity and compliance with study protocols.
Informed Consent Process:Explain the research study to participants and obtain informed consent.
Maintain documentation of informed consent processes.
Clinical Procedures: Assist with clinical procedures, including administering medications, medical tests, and assessments as per the study protocol.
Ensure adherence to ethical and safety standards.
Data Management:Enter, manage, and analyze research data using electronic databases and software.
Generate reports and assist in data interpretation.
Regulatory Compliance:Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines.
Assist in preparing and submitting regulatory documents as needed.
Study Coordination:Collaborate with principal investigators, physicians, nurses, and other healthcare professionals involved in the research.
Coordinate study-related activities and scheduling.
Participant Follow-up:Maintain regular contact with study participants to track their progress and ensure retention in the study.
Quality Assurance:Assist in monitoring and auditing study sites to ensure protocol adherence and data quality.
Adverse Event Reporting:Promptly report adverse events and safety concerns to the appropriate regulatory bodies.
Job Type: Full-time
Pay: $12.00 - $16.00 per hour
Benefits:
Schedule:
Experience:
Work Location: In person
Full Time
Wholesale
$53k-70k (estimate)
03/27/2024
05/26/2024
springclinicalresearch.com
Houston, TX
<25
Wholesale
The job skills required for Clinical Research Assistant include Clinical Research, Clinical Trial, Coordination, Data Collection, Data Management, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research 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. 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 positions, which can be used as a reference in future career path planning. As a Clinical Research 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. You can explore the career advancement for a Clinical Research 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.
01/02/2022: Vincennes, IN
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.