Top 3009 Conference account coordinator Jobs

Regulatory Coordinator
CenExel Clinical Research —Hollywood, FL
- Overtime
- Background check
- Microsoft Excel
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Financial Aid Coordinator
Charter College —Remote
- $25.00 - $30.05 an hour
- Full-time
- Mid-level
- Finance
- Associate's degree
Quick Apply
12d
Institutional Giving Coordinator
AWP Community Integration —Remote
- $55,000 - $60,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Research
- Health savings account
- Health insurance
Quick Apply
10d
Cancer Conference Coordinator
Work from Home —Nashville, TN
- Full-time
- Remote
- Mid-level
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Account Coordinator
BookBub —Boston, MA
- $52,000 - $55,000 a year
- Part-time
- Remote
- Research
- Communication skills
- Marketing
- Paid parental leave
- Health insurance
13d
Wholesale Sales Coordinator
Bellroy —Colorado Springs, CO
- $55,000 - $65,000 a year
- Full-time
- Remote
- Mid-level
- Analysis skills
- 2 years
- Paid parental leave
- Paid holidays
Coordinator Residency
Community Medical Center —Toms River, NJ
- $48,000 - $67,200 a year
- Full-time
- Mid-level
- Bachelor's degree
- 2 years
- Paid parental leave
- Paid holidays
Research Compliance Coordinator
University of the Incarnate Word —San Antonio, TX
- $63,000 - $65,000 a year
- Extended hours
- Microsoft Outlook
- Mid-level
- Master's degree
- 403(b) matching
- AD&D insurance
Account Coordinator
Zimmerman Advertising —Fort Lauderdale, FL
- Microsoft Outlook
- Marketing
- Computer literacy
Quick Apply
Editorial Coordinator
Yale University —New Haven, CT
- $31.83 an hour
- Part-time
- Hybrid work
- Background check
- Mid-level
- Bachelor's degree
Quality Assurance Coordinator
BerryDunn —Portland, ME
- $68,000 - $72,000 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- 5 years
Research Coordinator
University of Pennsylvania —Philadelphia, PA
- $44,500 - $46,108 a year
- Full-time
- Hybrid work
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Research Administrative Coordinator
Cardiovascular Associates of America —Remote
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick Apply
Issue Resolution Specialist / Account Coordinator Hybrid
Sunitna River LLC —Remote
- Full-time
- Remote
- English
- Mid-level
- Analysis skills
- Disability insurance
- Health insurance
Quick Apply
Assessment Coordinator
Texas A&M University —College Station, TX
- $5,000 a month
- 8 hour shift
- Microsoft Excel
- Microsoft Outlook
- Research
- AD&D insurance
- Paid holidays
11d
SEO Account Coordinator
Raleigh SEO Company —Raleigh, NC
- Marketing
- Research
- Office
- Paid time off
- Flextime
Account Executive
TriplePoint PR —Remote
- Full-time
- Research
- Business development experience
- Entry level
Film & TV Submissions & Programming Coordinator
SXSW, LLC. —Austin, TX
- Extended hours
- Mid-level
- Office
- Ability to lift 50 pounds
Quick Apply
7d
Fiscal and Grants Coordinator
Virginia Tech —Blacksburg, VA
- $55,000 - $65,000 a year
- Overtime
- Customer service
- Mid-level
- Finance
- Travel reimbursement
- Paid training
Account Coordinator (Evergreen)
Bauer Entertainment Marketing —Remote
- Full-time
- Remote
- Marketing
- Mid-level
- Bachelor's degree
- Dental insurance
- Vision insurance
Quick Apply

I want to receive the latest job alert for conference account coordinator

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

conference account coordinator jobs near

Financial Aid Coordinator jobs in Remote

Account Resolution Specialist jobs in Remote

Accounting Manager jobs in Blacksburg, VA

Account Coordinator jobs in Remote

Account Coordinator jobs in Raleigh, NC

Philanthropy Manager jobs in Remote

Sales Coordinator jobs in Colorado Springs, CO

Account Executive jobs in Remote

Conference Coordinator jobs in Nashville, TN

Account Coordinator jobs in Fort Lauderdale, FL

Administrative Coordinator jobs in Remote

Quality Assurance Coordinator jobs in Remote

Research Coordinator jobs in Philadelphia, PA

Account Coordinator jobs in Boston, MA

Compliance Officer jobs in San Antonio, TX

Entry Level Financial Analyst jobs in Lexington, KY

Financial Aid Coordinator jobs in Towson, MD

Hearing Aid jobs in San Diego, CA

Hearing Aid Specialist jobs in North Carolina

Financial Aid Coordinator jobs in Knoxville, TN

Regulatory Coordinator

CenExel Clinical Research -
Hollywood, FL

Quick Apply

Job Details

Full-time

Benefits

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

Qualifications

Computer operation
Microsoft Excel
Clinical research
Word processing
Writing skills
Drug regulation
High school diploma or GED
Regulatory affairs
Typing

Full Job Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

With moderate oversight the Regulatory Coordinator I is responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiation, execution, and reporting on the various status of research tasks in accordance with FDA guidelines, ICH GCP and SOPs. Maintain regulatory documents in accordance with applicable regulations and coordinate required investigator and study staff training.

Essential Responsibilities and Duties:

Collects, prepares, and submits documentation to various sponsors/CROs during study start-up, including:
o Submission documents/approvals
o Protocol amendments with respective signature pages
o Informed consent documents
o FDA form 1572
o Lab normal result documents
o financial disclosure forms
o Delegation of authority logs
o Licenses
o Reports
o Logs (e.g., temperature logs, drug accountability logs, master subject logs, screening and enrollment logs, specimen logs, etc.)
Collects, prepares, and submits documentation to institutional review boards for all ongoing and new trials.
Serve as a liaison between the IRB, site, and investigator.
Obtain necessary signatures from investigators and staff.
Maintains and tracks current staff credentials (i.e., CV, certifications, etc.)
Maintains and distributes new and revised regulatory documents to applicable site staff and applicable corporate teams.
Refers necessary regulatory questions to Sr. Regulatory Coordinator, Regulatory Manager or Regional Regulatory Manager.
Maintains regulatory documents for ongoing trials, and ensures all appropriate regulatory documents are archived at the conclusion of the study.
Submits applicable subject facing documents for translations.
Maintains current Clinical Conductor Regulatory information.
Prepares appropriate reports for submission as required to the IRB including Serious Adverse Events (SAE’s), protocol deviations and other required reports.
Completes onboarding of new Investigators, including CV creation, obtaining medical license, and training documents.
Ensures the regulatory binder is ready for monitor review during monitor visits. Meets with monitor, as necessary.
Assists with regulatory inspections and sponsor audits as necessary.
Performs close-out duties including preparing the final report to the IRB and ensuring all original documents are filed in the regulatory binder. Ensures all appropriate regulatory documents are archived at the conclusion of the study.
Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

Must be a high school graduate or have GED equivalency.
0-2 years of experience in clinical research regulatory affairs.
Demonstrated prioritization and organizational skills to efficiently and effectively, providing accurate information in a timely manner.
Ability to prioritize workload to meet demands of PI, coordinators, sponsors, and IRBs.
Demonstrated interpersonal skills to work with physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
Ability to understand work may be delegated by more than one person, depending on the individual needs of the clinical study and to carry out job responsibilities as assigned in a timely manner.
Computer skills using PC platform computers with proficiency in Excel and Word to enter data and generate correspondence accurately.
Ability to learn and become proficient in eRegulatory systems, IRB portals, vendor portals and sponsor portals.
A critical thinker with strong attention to detail and superb problem-solving abilities.
Must be able to effectively communicate verbally and in writing.

Working Conditions

Indoor, Office environment.
Essential physical requirements include sitting, typing, standing, and walking.
Lightly active position, occasional lifting of up to 20 pounds.
Reporting to work, as scheduled, is essential.
Ability to work overtime, weekends, and/or holidays as needed.
Ability to travel as needed.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Benefits:

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

Experience:

Clinical research: 1 year (Required)
Regulatory : 1 year (Required)

Work Location: In person

Quick Apply

Refine Your Search

conference account coordinator jobs

Regulatory Coordinator

Financial Aid Coordinator

Institutional Giving Coordinator

Cancer Conference Coordinator

Account Coordinator

Wholesale Sales Coordinator

Coordinator Residency

Research Compliance Coordinator

Account Coordinator

Editorial Coordinator

Quality Assurance Coordinator

Research Coordinator

Research Administrative Coordinator

Issue Resolution Specialist / Account Coordinator Hybrid

Assessment Coordinator

SEO Account Coordinator

Account Executive

Film & TV Submissions & Programming Coordinator

Fiscal and Grants Coordinator

Account Coordinator (Evergreen)

I want to receive the latest job alert for conference account coordinator

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected