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AdventHealth Altamonte Springs
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Clinical Research Assistant
AdventHealth Altamonte Springs Altamonte Springs, FL
$58k-75k (estimate)
Full Time 0 Months Ago
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AdventHealth Altamonte Springs is Hiring a Clinical Research Assistant Near Altamonte Springs, FL

Description

All the benefits and perks you need for you and your family:
  • Benefits from Day One
  • Paid Days Off from Day One
  • Student Loan Repayment Program
  • Career Development
  • Whole Person Wellbeing Resources
  • Mental Health Resources and Support
  • Pet Insurance*
  • Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)
Our promise to you:
Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.
Schedule:Full Time
Shift: Monday to Friday 8am - 5pm
Location: Altamonte Springs
The community you’ll be caring for:
  • Faith based & mission driven organization
  • Central Florida’s premier multi-specialty medical group
  • Comprehensive Employee Benefits such as Educational Reimbursement
  • CREATION Health employee wellness and lifestyle programs
  • Positive working climate to support a work life balance
The role you’ll contribute:
The Clinical Research Assistant – Spine Health Institute (SHI) (CRA) will assist the Clinical Research Coordinators (CRCs) and may be required to oversee specific duties relevant to patients participating in investigator initiated, pharmaceutical, device, in-house, outpatient, and other trials for the clinical research physician investigators. Prepare forms and data documentation as requested consistent with assignment. Assist with preparation, monitoring and follow-up of patient activities or regulatory processes as related to study requirements. Resolve queries issued by sponsor within a timely manner. Adhere to all AdventHealth, State of Florida, and federal regulations and guidelines pertaining to HIPAA. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all.
The value you’ll bring to the team:
  • Conforms to all standards of good research practice and provide support to the research department staff and patients by abiding by current IRB, FDA, federal, state, and institutional regulations pertaining to human subject’s research, including the use of institutional and departmental SOP’s.
  • Coordinates chart preparation and building patient profiles for all patients for protocol completions. This includes retrieving all new patient templates, entering appropriate physical exam templates into system, and exporting data for providers as well as disbursing templates to front staff for next clinic.
  • Enters all initial diagnosis, radiologic findings, and surgery information for patients. Ensures informed consents are in the database, documents the informed consent process, and files all informed consents for storage. Manages stored records per IRB protocol.
  • Facilitates study-required patient and/or regulatory activities of the trial according to the direction of manager or CRCs.Communicates incoming data and patient status such as adverse events and inconsistencies with the CRC.Responsible for accurate and timely submission of study related documents and materials.
  • Meets face to face with patients to complete assessments
Qualifications


The
expertise and experiences you’ll need to succeed:

EDUCATION AND EXPERIENCE REQUIRED:
  • 1 year of experience in a healthcare setting
EDUCATION AND EXPERIENCE PREFERRED:
  • Bachelor’s degree in healthcare related field
LICENSURE, CERTIFICATION, OR REGISTRATION PREFERRED:
  • Certification from a clinical research professional organization, eg. Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP)
This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.

Job Summary

JOB TYPE

Full Time

SALARY

$58k-75k (estimate)

POST DATE

04/19/2023

EXPIRATION DATE

05/10/2024

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The job skills required for Clinical Research Assistant include Clinical Research, Customer Service, Mental Health, 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.

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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.

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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

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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.

12/27/2021: Everett, WA

Step 3: View the best colleges and universities for Clinical Research Assistant.

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