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The Clinical Research Assistant will be responsible for assisting in the coordination of pediatric clinical research studies for the Delaware Valley Clinical Research Team.
The job includes but is not limited to: screening patients for study eligibility, scheduling research visits/follow up, tracking/auditing consent forms and study related documents, preparation for both internal and external audits, collecting data and submitting to appropriate organizations, processing/packaging of lab specimens, maintaining inventory of research supplies, creating electronic research charts, scheduling site monitor visits and meeting rooms as needed and assisting in the implementation of new laboratory protocols and processes.
This is a fast- paced working environment involving time sensitive specimens and hard deadlines for data submissions. A high level of organization with attention to detail and the ability to manage multiple responsibilities is required.
This position will work with multiple departments and must maintain a high level of professionalism and a continuous process improvement mindset.
The Clinical Research Assistant will be required to complete Human Subjects Protection (HSP) training and CITI training (including Good Clinical Practice (GCP).
Qualifications:
Essential Functions:
1. Prepare and maintain regulatory aspects of a study protocol from start to finish including preparation of regulatory start- up packets for research grants and pharmaceutical companies.
2. Screens patients for study eligibility by attending meetings and utilizing the electronic health record EPIC.
3. Recruit patients for studies to include: preparation and advertising requests and interviewing patients to determine appropriateness for research study.
4. Preparing patient notebooks/binders, recording and maintaining accurate data in research notebooks/binders, developing data collection tools, collecting data, monitoring and ordering supplies (registries and retrospective studies).
5. Interact with Principal Investigators, research study team, and study monitors.
6. Compliance with minimal research training (human subjects protection, good clinical practice, and Nemours University).
7. Assist with stipend request for patients.
8. Assist with specimen preparation and shipping.
9. Develops strategies to ensure study subject compliance with protocol requirements.
Full Time
$74k-100k (estimate)
04/12/2023
06/18/2024
The job skills required for Clinical Research Assistant include Clinical Research, Analysis, Data Collection, Scheduling, Data Entry, 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.
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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.
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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.
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Research Assistants provide support to research teams who are conducting experiments or gathering and analysing data.
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Maintained FDA clinical trial documentation for department and received excellent FDA audits of records.
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Have strong customer focus and good communication skills
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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.
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Step 3: View the best colleges and universities for Clinical Research Assistant.