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M Chest Pharmacy

<div>
 
 Job Description
 
 
 
 Texas based LTC Pharmacy is seeking a Full-Time Pharmacy Technician to become a part of our Pharmacy team!
 
 
 We are seeking a dedicated Pharmacy Technician who thrives in a fast-paced, high-volume environment with minimal supervision. If you&rsquo;re driven, detail-oriented, and ready to take initiative while juggling multiple priorities, we want you on our team.
 
 
 
 Schedule:
 
 
 
 
 Full Time:
 
 Monday thru Friday 10 am - 7 pm or 11 am - 8 pm
 
 
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 Rotating Saturday &amp; Sunday schedule (every other week)
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 Days off occurs during the week when working Saturday &amp; Sunday
 
 
 
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 Note
 
 : Must be agreeable to a modified schedule during training, regular schedule will resume once training is complete
 
 
 
 
 Responsibilities:
 
 
 
 
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 Triage incoming Rx orders.
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 Accurately enter Rx orders according to pharmacy workflow and delivery cut-off times.
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 Process refills as requested.
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 Process 3rd party claims adjudication (insurance claims rejections).
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 Coordinate and triage all pharmacy inquiries (i.e. phone, fax, correspondence, electronic media) and resolve all customer issues; ensuring accurate information is provided.
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 Outreach to Retail Pharmacies and delivery service to coordinate filling of medications in between scheduled pharmacy deliveries.
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 Resolve customer complaints in a timely, accurate and professional manner.
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 Provide customers with resources or additional information.
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 Navigate across multiple computer systems to respond to questions from external and/or internal partners.
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 Constantly meet established productivity requirements, schedule adherence and quality standards.
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 Handle incoming and outgoing calls related to prescription orders, refills, and patient inquiries.
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 Verify and input prescription information accurately into the pharmacy system.
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 Assist patients and healthcare providers with medication-related questions and provide clear, professional guidance.
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 Work closely with pharmacists and other technicians to ensure timely and accurate prescription processing.
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 Maintain a high level of accuracy when collecting and documenting patient information.
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 Monitor order statuses, provide updates, and resolve any issues that may arise with prescriptions or shipments.
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 Ensure compliance with all pharmacy laws, regulations, and company policies
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 Maintain patient confidentiality and adhere to HIPAA regulations.
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 Other duties as assigned.
 
 
 
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 Required Qualifications
 
 
 
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 Unblemished TSBP Pharmacy Technician Registration in good standing
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 One (1) year of high-volume order entry required
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 Experience in Long Term Care pharmacy
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 Must be able to demonstrate a working knowledge of a PC and be able to learn and use new software
 
 
 
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 Preferred Qualifications
 
 
 
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 Experience with Framework, Docutrack or ECM preferred
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 Remote work
 
 
 
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 Job Type:
 
 Full Time
 
 
 
 Benefits:
 
 
 
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 401(k)
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 401(k) matching
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 Medical, Dental and Vision
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 Short-Term disability
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 Critical Illness
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 Accident Insurance
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 Life Insurance
 
 
 
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 Education:
 
 High school or Equivalent (Preferred)
 
 
 
 License/Certification:
 
 
 
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 Texas State Board of Pharmacy Registration (Required)
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 Driver's License (Preferred)
 
 
 
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 Work Location:
 
 Remote
</div>

Pharmacy Technician - Day Shift

Gritter Francona

<div>
 Gritter Francona, Inc. is seeking a versatile Management Analyst to manage multiple initiatives and lead project management and project control/planning activities across various business process modeling and information modeling projects. This role may also include overseeing and managing strategic planning and multi-year programming, coordinating the activities related to capability management boards, ensuring effective communication and alignment of strategic goals, and providing comprehensive project management support. The Management Analyst will work closely with leadership, board leads, and other stakeholders to drive the successful execution of initiatives.
 
 
 Key Responsibilities:
 
 
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 Lead and manage program management tasks, ensuring alignment with strategic goals.
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 Develop and manage comprehensive project plans, schedules, and deliverables for strategic planning and MYP.
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 Coordinate and facilitate meetings, briefings, and decision-making processes.
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 Ensure alignment of IT strategy with directives through comprehensive reporting and analysis.
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 Support the development and management of business cases, multi-year programming, and investment monitoring.
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 Facilitate strategic planning sessions and workshops with leadership.
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 Identify and mitigate project risks, ensuring timely resolution of issues.
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 Provide regular updates on task progress, milestones, and outcomes to executive leadership.
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 Maintain and manage documentation, critical artifacts, and project deliverables.
 
 
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 Requirements
 
 
 
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 Bachelor's degree in project management, Business Administration, Information Technology, or related field.
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 Minimum 4 years of experience, preferably project management experience within the healthcare or government sector.
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 Strong analytical, organizational, and leadership skills.
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 Excellent written and verbal communication skills.
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 Proficiency in project management tools and software, including Microsoft Project and SharePoint.
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 Ability to manage multiple projects and priorities effectively.
 
 
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 Preferred Qualifications:
 
 
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 PMP or similar project management certification
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 Knowledge of strategic planning and multi-year programming processes
 
 
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 Benefits
 
 
 
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 Health Care Plan (Medical, Dental &amp; Vision)
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 Retirement Plan (401k, IRA)
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 Life Insurance (Basic, Voluntary &amp; AD&amp;D)
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 Paid Time Off (Vacation, Sick &amp; Public Holidays)
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 Short Term &amp; Long Term Disability
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 Training &amp; Development
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</div>

Management Analyst

ICON Strategic Solutions

<div>
 Clinical Research Associate - Early Development Multi Therapeutic - Midwest Region
 
 
 ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
 
 
 
 What You Will Be Doing
 
 
 
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 Serve as the primary point of contact between investigation sites and the sponsor
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 Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
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 Ensure site compliance with ICH-GCP, SOPs, and regulations
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 Maintain up-to-date documentation in CTMS and eTMF systems
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 Support and track site staff training and maintain compliance records
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 Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
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 Support subject recruitment and retention efforts at the site level
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 Oversee drug accountability and ensure proper storage, return, or destruction
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 Resolve data queries and drive timely, high-quality data entry
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 Document site progress and escalate risks or issues to the clinical team
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 Assist in tracking site budgets and ensuring timely site payments (as applicable)
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 Collaborate with cross-functional partners including CTAs, LTMs, and CTMs
 
 
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 You Are
 
 
 
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 A graduate with a Bachelor&rsquo;s degree in Life Sciences or equivalent, or a qualified RN
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 Eligible to work in United States without visa sponsorship
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 A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
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 Experienced monitoring early development Phase I/II clinical studies, across multiple therapeutic areas
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 Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
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 A clear communicator, problem-solver, and collaborative team player
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 Willing and able to travel up to 60% for on-site monitoring visits across the Midwest region; preference given to candidates residing in Midwest region near major HUB airports to support efficient regional travel
 
 
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 What ICON Can Offer You
 
 
 
 Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
 
 
 In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
 
 
 
 Our Benefits Examples Include
 
 
 
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 Various annual leave entitlements
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 A range of health insurance offerings to suit you and your family&rsquo;s needs.
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 Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
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 Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family&rsquo;s well-being.
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 Life assurance
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 Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
 
 
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 Visit our careers site to read more about the benefits ICON offers.
 
 
 At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
 
 
 If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
 
 
 Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.
 
 
 Are you a current ICON Employee? Please click here to apply
</div>

Clinical Research Associate

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3 ai training mathematics jobs In Texas

Pharmacy Technician - Day Shift

Management Analyst

Clinical Research Associate