Top 16 Clinical research coordinator Jobs in Deland Fl

Clinical Research Coordinator
Alcanza Clinical Research —DeLand, FL
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
3d
Clinical Research Assistant/Pharmacy Tech
Cardiovascular Associates of America —Daytona Beach, FL
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Mid-level
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8d
Oncology Research Coordinator
Halifax Health —Daytona Beach, FL
- Full-time
- Hospital
- Customer service
- Writing skills
6d
Special Projects Coordinator - Clinical Assistant to the Medical Director
Volusia County, FL —Holly Hill, FL
- $65,769.60 a year
- Full-time
- Management
- Writing skills
- HIPAA
- Paid holidays
- Disability insurance
Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site)
Fortrea —Daytona Beach, FL
- Full-time
- CPR Certification
- Nursing
- Bachelor of Science
- Disability insurance
- Health insurance
Registered Nurse Clinical Coordinator Emergency
HCA Florida Lake Monroe Hospital —Sanford, FL
- Full-time
- Mid-level
- Pediatrics
- Employee stock purchase plan
- Disability insurance
Quick Apply
10d
RN Clinical Improvement Coordinator
AdventHealth Fish Memorial —Orange City, FL
- $31.82 - $59.17 an hour
- Full-time
- CPR Certification
- Nursing
- Management
- Paid parental leave
- Disability insurance
Director/Senior Director, Clinical Research Volunteer/Participant Recruitment & Engagement
Fortrea —Daytona Beach, FL
- Full-time
- Master's degree
- Continuous improvement
- Experience equivalent to degree accepted
8d
Clinical Research Physician - Psychiatrist (Part time)
Alcanza Clinical Research —DeLand, FL
- Part-time
- Spanish
- Medicine
- Psychiatry
- Health savings account
- Disability insurance
Quick Apply
Registered Nurse- Clinical Coordinator (Orthopedics)
Halifax Health —Daytona Beach, FL
- Full-time
- Nursing
- RN License
- Mid-level
Clinical Nurse Coordinator Cardiac Neuro East CNC
HCA Florida Lake Monroe Hospital —Sanford, FL
- Full-time
- Mid-level
- Neurology
- Cardiology
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Nurse Coordinator Cardiac Neuro CNC
HCA Florida Lake Monroe Hospital —Sanford, FL
- Full-time
- Mid-level
- Neurology
- Cardiology
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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Clinical Research Assistant/Pharmacy Tech
Cardiovascular Associates of America —Daytona Beach, FL
Associate's or Bachelor's degree in a health science, biological science, or related field preferred. Support filing and organization of study records.
Quick Apply
8d
Clinical Research Coordinator
Alcanza Clinical Research —DeLand, FL
Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical…
Quick Apply
3d

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Clinical Research Coordinator-Clinical Trials Management Office
The Ohio State University Wexner Medical Center —Columbus, OH
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer…
1d
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Coordinator

Alcanza Clinical Research -
DeLand, FL

Quick Apply

Job Details

Full-time
3 days ago

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Vision insurance
401(k) matching
Life insurance

Qualifications

Computer operation
Laboratory procedures
Electronic health records (EHR) management
HIPAA
Health information regulatory compliance
Typing
Data collection
Clinical confidentiality policies

Full Job Description

Description

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Key Responsibilities

Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:

Screening of patients for study enrollment;
Patient consents;
Patient follow-up visits;
Documenting in source clinic charts;
Entering data in EDC and answers queries;
Obtaining vital signs and ECGs;
May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
Requesting and tracking medical record requests;
Updating and maintaining logs, chart filings;
Maintaining & ordering study specific supplies;]
Scheduling subjects for study visits and conducts appointment reminders;
Building/updating source as needed;
Conducting monitoring visits and resolves issues as needed in a timely manner;
Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
Filing SAE/Deviation reports to Sponsor and IRB as needed;
Documenting and reporting adverse events;
Reporting non-compliance to appropriate staff in timely manner;
Maintaining positive and effective communication with clients and team members;
Always practicing ALCOAC principles with all documentation;
May assist with study recruitment, patient enrollment, and tracking as needed;
Maintaining confidentiality of patients, customers and company information, and;
Performing all other duties as requested or assigned.
Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
May set up, train and maintain all technology needed for studies.

Skills, Knowledge and Expertise

Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate’s degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. Bi-lingual (English / Spanish) proficiency is a plus.

Required Skills:

Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
Strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
Must be professional, respectful of others, self-motivated, and have a strong work ethic.
Must possess a high degree of integrity and dependability.
Ability to work under minimal supervision, identify problems and implement solutions.
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits

Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

About Alcanza Clinical Research

Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all.

We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these new therapies, and the entire medical community. Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life.

Alcanza is a culturally competent organization. We treat each other with dignity, creating an environment where all individuals feel welcome, heard, and respected for their unique perspectives and aspirations. We put considerable effort into finding exceptional employees who mirror the values most important to us: Inclusive, Impactful, Compassionate, and Determined.

Alcanza Clinical Research is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company.

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Refine Your Search

clinical research coordinator jobs in deland fl

Clinical Research Coordinator

Clinical Research Assistant/Pharmacy Tech

Oncology Research Coordinator

Special Projects Coordinator - Clinical Assistant to the Medical Director

Clinical Research Nurse, Early Phase Clinical Trials - Daytona Beach, FL (On-Site)

Registered Nurse Clinical Coordinator Emergency

RN Clinical Improvement Coordinator

Director/Senior Director, Clinical Research Volunteer/Participant Recruitment & Engagement

Clinical Research Physician - Psychiatrist (Part time)

Registered Nurse- Clinical Coordinator (Orthopedics)

Clinical Nurse Coordinator Cardiac Neuro East CNC

Clinical Nurse Coordinator Cardiac Neuro CNC

Clinical Donation Coordinator I - PeeDee Region

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Description

Key Responsibilities

Skills, Knowledge and Expertise

Benefits

About Alcanza Clinical Research

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