Sr. Quality Specialist, Clinical Quality Job at Baptist Health (Florida) (Fleming Island, FL)

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Sr Clinical Data Analyst

Access and analysis of clinical and quality data is critical to optimizing patie...

Location

United States , Cleveland

Salary:

65104.00 - 101774.40 USD / Year

University Hospitals

Expiration Date

Until further notice

Requirements

Bachelor’s Degree (Required)
Master’s Degree In data science or data analytics (Preferred)
Experience within a healthcare environment (Preferred)
5+ years Experience in relevant data/analytics field (Required)
Microsoft Office and excel experience (Required)
Quality & Process Improvement skills (Required proficiency)
Written & verbal communication skills (Required proficiency)
Organizational skills (Required proficiency)
Power BI (Preferred proficiency)
QI Macros (Preferred proficiency)

Job Responsibility

Performs concurrent & retrospective electronic data collection from clinical and operational databases, optimizes integration of data from multiple data systems
Analyzes clinical and operational data, develops summary reports / dashboards and recommendations, control charts / graphs, trends outcomes, identifies opportunities for improvement, collaborates with team members, and supports recommendations with data and judgment
Supports and facilitates clinical and quality improvement initiatives in collaboration with domain specialists through meeting attendance, data preparation, leading analytical discussions, effective written/verbal communication skills, professional interpersonal skills
Maintains optimal communication with management regarding data requests
Leads analytical training/education for teams, mentors staff, presents outcomes to leadership and physicians, identifies and corrects data errors, proactively communicates opportunities for improvement, establishes positive relationships with other departments, and serves as a primary resource for the data analytics team within the UH System of care
Performs other duties as assigned
Complies with all policies and standards
Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients

What we offer

healthcare
dental
vision
retirement plan options

Fulltime

Sr. QA Specialist - Ops

The Sr. QA Specialist – Team Lead will work with other departments to ensure the...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

7-9 years of pharmaceutical or biotech industry
4+ years of experience in a QA Operations role supporting late stage clinical and/or commercial production
Bachelor’s Degree in a relevant scientific discipline preferred
Experience performing RCA, technical writing, and working with quality related investigations
Knowledge of laboratory and production equipment and IQ/OQ/PQ
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH
Experience using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9
Ability to Travel 10%

Job Responsibility

Perform review of batch documentation for release of internal and external clinical products/commercial products, while ensuring compliance with cGMPs, site SOPs, and regulatory requirements. Prioritize record review in support of business needs including maintaining batch status and communicate release needs throughout the organization
Review and approve master batch records for the timely initiation of GxP manufacturing activities
Responsible for quality oversight and administration of the deviation/investigation and CAPA programs
Review and approve Manufacturing, Quality Control, and other investigations in support of batch release and GMP compliance
Provide direction for complex investigations and CAPAs
Ensure timely, accurate and complete execution and documentation of quality system events: deviations, NCMRs, GxP investigations and CAPAs
Review, develop, and improve quality system procedures, specifications, and test methods
Review and approve CAPAs to prevent recurrence of deviations
Review and approve Change Control documentation
Responsible for tracking investigations and change control for timely completion. Provide status reports, including relevant quality metrics and participate in the management review process

Fulltime

New

Material Receiving Inspector (Mechanical)-QCI

Material Receiving Inspector (Mechanical) checks and guarantees that certificate...

Location

Saudi Arabia , Jubail

Salary:

Not provided

Met T&S

Expiration Date

Until further notice

Requirements

A university degree or diploma in a relevant discipline, or an equivalent qualification in Mechanical Engineering
Relevant experience in construction/modernization of oil & gas /industrial sector/ EPC projects large refinery plants
At least 10 years of experience in the specific discipline
Experience working on Main Contractor side
Fluent English
Excellent IT and analytical skills
Attention to detail, excellent communications skills
Strong interpersonal, team-oriented skills, self-motivation, and direction, with strong bias toward timely performance and problem resolution

Job Responsibility

Knowledge and experience of material receiving and inspection as per Client’s procedures
To forward materials to Subcontractors, according to the instructions given by the Material Controller
To keep records about the handling of materials, using the Company software systems
To perform feasibility analysis by the Company software system
To maintain the inventory of unused material for sale
To have general Mechanical QCI background (Metallic/ Non-Metallic Piping, Valves, Hydrotesting, Coating)

What we offer

Competitive Salary package with benefits

Fulltime

New

Duty Manager

Process all guest check-ins, verifying guest identity, form of payment, assignin...

Location

Vietnam , Danang

Salary:

Not provided

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

High school diploma or G.E.D. equivalent
At least 1 year of related work experience
At least 1 year of supervisory experience

Job Responsibility

Process all guest check-ins, verifying guest identity, form of payment, assigning room, and activating/issuing room key
Set up accurate accounts for each guest according to their requirements
Enter Marriott Rewards information
Ensure rates match market codes, document exceptions
Secure payment prior to issuing room key, verify/adjust billing
Compile and review daily reports/logs/contingency lists
Complete cashier and closing reports
Supply guests with directions and property information
Accommodate guest requests, contacting appropriate staff if necessary
Follow up to ensure requests have been met

Fulltime

New

Account Manager

We’re a game changer that optimizes supply chains of the world’s leading compani...

Location

The Netherlands , Rotterdam

Salary:

Not provided

OMP

Expiration Date

Until further notice

Requirements

10+ years of account management experience
At least a bachelor’s degree, preferably a master’s degree
A track record of top performance in supply chain software solutions for manufacturing companies
The proven ability to build trust from senior-level management and managers
A customer-centric mindset and an entrepreneurial approach
The ability to clearly articulate your viewpoint to all levels of customers and management
Experience with CRM solutions such as Salesforce.com
Strong ability to lead by example with proficiency in one or more of our core industries
English language

Job Responsibility

Developing outstanding customer partnerships focused on the entire customer life cycle
Building and managing long-lasting relationships with multiple levels of stakeholders
Understanding our customers’ industry and business situation, concerns, and needs
Communicating your customers’ needs and concerns to the internal teams (delivery, marketing, etc.)
Articulating and developing an account strategy in line with OMP culture and strategy, including short-, mid- and long-term action plans
Mapping stakeholders using organization charts of customer leadership and teams
Aligning with the project team during all project phases through optimized governance
Maximizing customer engagement and retention by increasing OMP awareness and mindshare at the customer
Guiding customers toward optimal use of the solution by being the go-to contact after project delivery
Preparing and running account management meetings to assess customer needs, review scorecards, and share relevant content

What we offer

Access customized training, coaching programs, and on-the-job development opportunities
Flex your schedule with working from home, adaptable hours, and the autonomy to shape your routine
An attractive salary package including an optional company car, a bike incentive program, additional extralegal vacation days, and other competitive benefits
Cross-team collaboration and creative challenges that encourage you to share knowledge, celebrate wins, and grow together
Encouragement to think differently through cross-team collaboration and innovation challenges
A workplace that supports your physical and mental health by promoting a wide range of facilities and activities like birthday events, sports sessions, in-house coaches, and healthy meal options

New

Civil Project Engineer

TAIT is seeking a Civil Design Project Engineer to join our Loveland, CO office....

Location

United States , Loveland

Salary:

75000.00 - 95000.00 USD / Year

TAIT & Associates, Inc

Expiration Date

Until further notice

Requirements

B.S. in Civil Engineering
3–5 years of experience in civil engineering design
Proficiency with AutoCAD (2009 or newer), Civil 3D, and hydrology/hydraulics software
Excellent written and verbal communication skills
E.I.T. certification preferred
Occasionally walk job sites and carry or use survey equipment
Ability to drive to job locations as needed

Job Responsibility

Manage and coordinate design engineers to meet project objectives
Develop construction documents using AutoCAD and Civil 3D, transforming conceptual designs into detailed plans
Design horizontal and vertical alignments, perform earthwork calculations, and prepare profiles and cross sections
Create plans for grading, drainage, street improvements, water, sewer, and storm drain systems
Prepare engineering drawings, constraint maps, and special exhibits based on field data and research
Ensure deliverables meet project specifications, regulatory standards, and client expectations

What we offer

Flexible Work Schedule Options - Remote, Hybrid, In-Person
Medical options including PPO and HDHP with Health Savings Accounts (no extra charges for spouse or dependent coverage)
Dental Plans with little to no deductible
Vision PPO plan
Company paid Life Insurance
ID Theft Protection & Monitoring
Voluntary Life, Accident and Critical Illness plans
Dependent Care and Flexible Spending Accounts
Employee Assistance Program
Retirement plan 401(k) with employer match

Fulltime

New

Corporate Sales Executive

Location

Qatar , Doha

Salary:

Not provided

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

Proven corporate sales experience within the Qatar market
Bachelor’s degree in Business Administration, Marketing, or a related field
Strong background in corporate sales within reputable international hotel brands (Marriott experience preferred)
Demonstrated success in driving corporate revenue within the hospitality sector
Solid experience working with recognized luxury or upscale hospitality brands
Excellent negotiation, communication, and interpersonal skills
Ability to build and sustain long-term relationships with corporate clients and stakeholders
Proficiency in Opera PMS and related hospitality systems
Valid Qatar driving license (required)

Job Responsibility

Execute corporate sales strategies and manage daily sales activities to achieve revenue targets
Identify, approach, and secure new corporate accounts and business opportunities
Develop and maintain strong relationships with existing corporate clients to maximize revenue
Support the planning and execution of strategic and tactical sales initiatives aligned with business goals
Conduct market research to stay informed on industry trends, competitor activity, and market dynamics
Prepare and deliver professional sales presentations, proposals, and contractual agreements
Collaborate with marketing and operations teams to enhance brand visibility within target segments
Maintain accurate records and reports using hotel sales and property management systems

What we offer

Competitive salary based on experience

Fulltime

Sr. Quality Specialist, Clinical Quality

Baptist Health (Florida)

Location:
United States , Fleming Island, FL

Category:
Nursing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 10, 2026

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