clinical risk manager

NMC healthcare LLC

<h2>Job Description</h2><p><u>Specific Responsibilities for this Role</u></p><ul><li>Provide a comprehensive professional and ethical quality clinical services to patients in an effective and efficient manner.</li><li>Monitor and manage clinical risks associated with direct patient care.</li><li>Ensure compliance with clinical governance and quality management standards.</li><li>Maintain accurate medical records.</li><li>Ensure excellence in medical practice is maintained by focusing on continuous professional development of self and others.</li><li>Maintain integrity in professional services by executing clinical services in an ethical and responsible manner</li></ul><p><u>Occupational Safety and Health Management Systems</u></p><ul><li>Comply with reasonable OSH instructions, policies and safe working procedures</li><li>Use of appropriate personal protective equipment and safety systems.</li><li>Be familiar with emergency and evacuation procedures</li><li>Not willfully or recklessly endanger anyone’s health and safety</li><li>Assist with the preparation of risk assessments</li><li>Report OSH Hazards, incidents, Near misses and issues</li><li>Reduce, Reuse, Recycling of waste as much as possible</li><li>Attend all OSH Trainings, awareness programs and mock drills.</li><li>Participates in the OSHMS audits, inspections, ensuring standards are maintained</li></ul><p><u>Prevention and Control of Infection (PCI):</u></p><ul><li>PCI is everyone’s responsibility. All staff are required to read and implement the NMC PCI Policy and Strategy in an effort to maintain the highest possible standards of cleanliness at all times, thus reducing the risk of infection in patients, staff and visitors.</li></ul><p>The strictest hand hygiene, 5 moments of hand hygiene, bare below the elbows and environmental care, will be expected of all staff, including the post holder, at all times</p><h2>Responsibilities</h2>

Specialist - Endocrinology

TYG Consultant's

<p><b>Clinical Data Manager</b></p><p><b>100 percent onsite-Location: Maple Grove, MN</b></p><p><b>Hours: 8:00am-4:00 PM</b></p><p><b>Duration: This is a 6-month contract with potential to extend highly likely</b></p><p><b>Main purpose of role</b></p><p><b>Summarize the main purpose of the role.</b></p><p>The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk-based quality management systems, as described in the risk assessment, data management plan, and site and central monitoring plans.</p><p>As the customer-face of Data Review and its primary liaison with the therapy group, the Clinical Data Manager's therapy-specific knowledge ensures alignment to customer definitions of criticality, and informs review and analysis of study data.</p><p><b>Main responsibilities</b></p><ul><li>Identification of study specific risks to study conduct and human subject safety; analysis of risks; development and implementation of mitigation strategies.</li><li>Review of study data to detect anticipated and unanticipated issues related to trial data completeness and quality.</li><li>Facilitate multi-stakeholder discussions to review findings, evaluate impact and develop action plans for correction and continued monitoring.</li><li>Conduct Central Monitoring activities, as described in Central Monitoring Plan.</li><li>Direct all data cleaning activity related to assigned studies.</li></ul><p><b>Qualifications</b></p><ul><li>Bachelors Degree (&plusmn; 16 years) Biology, Health Sciences, Mathematics, Computer Science, or equivalent.</li></ul><p><b>Experience/Background</b></p><ul><li>Minimum 3 years</li></ul><p><b>Experience Details</b></p><ul><li>3 years in clinical operations or healthcare related field.</li><li>Education and work experience in project management, life sciences and/or technical field.</li><li>Knowledge of data collection best practices for clinical trials.</li><li>Knowledge of global clinical operations.</li><li>Experience in consultative role, with Subject Matter Expertise, and effectively influencing a team decision to the desired outcome.</li><li>Proficient at the identification of risks in a process, evaluation of likelihood and impact, and the development of effective mitigation and monitoring strategies that are imperfect yet meet the business need.</li><li>Proficient in the translation of clinical trial requirements to the technical specifications required for effective data collection.</li><li>Skilled at making inferences and connections based on limited information, clearly describing the knowns, unknowns, and alternative explanations.</li><li>Intermediate project management skills; developing a multifaceted plan with complex dependencies and holding peers accountable to adherence to the plan while maintaining positive and collaborative relationships.</li><li>Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device.</li></ul><p><b>Licenses and Certifications</b></p><ul><li>None required; Certified Clinical Data Manager (CCDM) or equivalent nice to have.</li></ul><p>Job Type: Contract</p><p>Pay: $42.00 - $44.00 per hour</p><p>Expected hours: 40 per week</p><p>Benefits:</p><ul><li>Health insurance</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>clinical data: 3 years (Preferred)</li><li>EDC (Electronic Data Capture): 3 years (Preferred)</li><li>central monitoring or risk-based monitoring: 3 years (Preferred)</li><li>pharma, medical device, CRO or healthcare industry: 3 years (Preferred)</li><li>overseeing clinical trial data: 3 years (Preferred)</li></ul><p>Ability to Commute:</p><ul><li>Maple Grove, MN 55311 (Preferred)</li></ul><p>Work Location: In person</p>

Clinical Data Manager (EDC/Clinical Operations/Central Monitoring) (Pharma/Healthcare)

Estithmar Holding

<div>
 <p>
  The role incumbent is responsible for auditing clinical and administrative processes to ensure adherence to healthcare quality standards, patient safety protocols, and regulatory compliance in a hospital setting. The role supports continuous quality improvement initiatives, risk management, and ensures that hospital practices align with national and international accreditation standards.
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <p>
  <strong>
   1. Quality Assurance &amp; Clinical Audits
  </strong>
 </p>
 <ul>
  <li>
   Conduct regular audits of clinical departments to assess compliance with evidence-based practices, clinical guidelines, and hospital policies.
  </li>
  <li>
   Analyze patient records, documentation, and outcomes to identify gaps in care or areas.
  </li>
  <li>
   Identify risks and opportunities for improvement in patient care processes.
  </li>
  <li>
   Evaluate adherence to hospital-wide quality metrics and KPIs.
  </li>
  <li>
   Monitor and report on key performance indicators (KPIs) related to quality and safety.
  </li>
 </ul>
 <p>
  <strong>
   2. Patient Safety
  </strong>
 </p>
 <ul>
  <li>
   Audit incident reports and investigate adverse events, near-misses, and sentinel events.
  </li>
  <li>
   Audit implementation of patient safety programs and protocols (e.g. hand hygiene, medication safety, surgical safety).
  </li>
  <li>
   Review and assess hospital compliance with national patient safety goals (e.g. WHO, JCI, or local health authority standards).
  </li>
 </ul>
 <p>
  <strong>
   3. Compliance &amp; Accreditation
  </strong>
 </p>
 <ul>
  <li>
   Ensure hospital practices align with national and international standards (e.g., MoPH, JCI, ISO)
  </li>
  <li>
   Perform compliance audits on medical records, infection control, consent processes, and other regulated areas.
  </li>
  <li>
   Review environmental safety measures.
  </li>
  <li>
   Audit documentation, incident reports and corrective actions for regulatory compliance.
  </li>
 </ul>
 <p>
  <strong>
   4. Reporting &amp; Documentation:
  </strong>
 </p>
 <ul>
  <li>
   Prepare detailed audit reports with findings, risk assessments and recommendations.
  </li>
  <li>
   Track corrective actions and verify their implementation and effectiveness.
  </li>
  <li>
   Present findings to hospital leadership and line manager.
  </li>
 </ul>
 <p>
  <strong>
   Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   <strong>
    Education:
   </strong>
   Bachelor&rsquo;s degree in Nursing or Medical degree, Health Sciences, Healthcare Administration, or related field (Master&rsquo;s preferred).
  </li>
  <li>
   <strong>
    Certifications:
   </strong>
  </li>
  <li>
   Patient Safety Certification (e.g. CPPS) is a plus
  </li>
  <li>
   Internal Auditor Certification (ISO or equivalent) preferred
  </li>
  <li>
   <strong>
    Experience:
   </strong>
  </li>
  <li>
   Minimum 3&ndash;5 years of experience in quality management, clinical auditing, or healthcare compliance.
  </li>
  <li>
   Experience in a JCI-accredited hospital or healthcare setting is an advantage.
  </li>
 </ul>
 <p>
  <strong>
   Skills &amp; Competencies:
  </strong>
 </p>
 <ul>
  <li>
   Strong knowledge of healthcare quality standards and patient safety principles
  </li>
  <li>
   Strong understanding of healthcare risk management
  </li>
  <li>
   Familiarity with accreditation frameworks (e.g. JCI, ISO, local health authority)
  </li>
  <li>
   Analytical and detail-oriented with excellent report writing skills
  </li>
  <li>
   Strong communication and interpersonal skills
  </li>
  <li>
   Ability to manage multiple audits and prioritize tasks
  </li>
  <li>
   Proficient in Microsoft Office, audit tools, and healthcare data systems
  </li>
 </ul>
</div>


Director Audit and Compliance – Clinical & Patient Safety

INSIGHTEC

<div><p>Insightec is a growing medical technology company transforming patient lives through innovative incisionless surgery.</p><p></p><p><br>
Our culture is as unique as our people, a diverse global team, with different ideas, skills, interests, and cultural backgrounds driven by our core values &ndash; Our Patients, Integrity, Team, Quality and Innovation.</p><p></p><p><br>
Our dedication to making a real impact on the lives of millions of people and paving the path to a bright future for healthcare, is what bonds us as a Team. We work together in a dynamic collaborative environment to deliver successfully while believing and driving a life-work balance philosophy that encourages our employees to do things that are meaningful outside of work. Every role is significant, your voice is heard, and your ideas are encouraged. We challenge and empower our people to be great at what they do while providing a flexible work environment.</p><p></p><p><br>
Walking through our corridors, you will be inspired by stories of career journeys at Insightec. We take pride in growing internal talent and encourage our employees to achieve their professional ambitions. With employees in Israel - Haifa and K. Ono, Miami and Dallas, Shanghai, Tokyo and Europe, we offer in each region competitive perks and benefits.</p><p></p><p><br>
Do the most meaningful work of your career by joining us on our mission to transform tomorrows, today.</p><p></p><p><br>
The Clinical Project Manager serves as the clinical trial lead and will lead clinical trial initiatives for Insightec. You will ensure trial compliance, regulatory alignment, and operational efficiency while collaborating with cross-functional teams such as Medical Affairs, R&amp;D, and Quality &amp; Regulatory to advance Insightec&rsquo;s clinical pipeline. The Clinical Project Manager is expected to independently manage the clinical trial by effectively planning and executing the study to ensure quality of deliverables within the specified budget and timeframe.</p><p></p><p><b><br>
Key Responsibilities:</b></p><ul><li>
Clinical Trial Management:</li><li>
Lead and manage multiple clinical trials from initiation through to completion, ensuring adherence to study timelines and budgets.</li><li>
Collaborate with investigators, vendors, and cross-functional teams to ensure study execution and operational excellence including implementation of best practices such as quality by design.</li><li>
Oversee the preparation and review of trial-related documentation, including protocols, informed consent forms (ICFs), case report forms (CRFs), and clinical study reports.</li><li>
Support creation of investigator brochures, clinical evaluation reports, publications and other documentation such as annual reports as applicable.</li><li>
In partnership with R&amp;D Program Management, develop and drive cross functional study timelines related to trial setup and execution</li><li>
Other roles/responsibilities will be defined as needed</li></ul><p>
Team Leadership:</p><ul><li>
Drive the cross functional internal study team ensuring appropriate alignment, risk management and coordination across all participating functions.</li><li>
Successfully interface with Data Management, Biostatistics and Clinical Monitors to ensure seamless monitoring and data cleaning initiatives to meet study deliverables and timelines</li><li>
Foster a collaborative team environment focused on operational efficiency and continuous improvement.</li><li>
Regulatory and Compliance Oversight:</li><li>
Ensure that clinical trials are conducted in compliance with all applicable regulations and ISO 14155 and ICH-GCP guidelines as applicable.</li><li>
Lead submissions of clinical trial documents to central IRB/IECs as applicable and ensure insurance and recruitment materials are prepared appropriately.</li><li>
Support the preparation and submission of clinical trial applications, including IDEs, PMAs, 501K, INDs, and other regulatory documents with functional leads from regulatory affairs.</li><li>
Manage interactions with Regulatory Affairs and external vendors to ensure timely submissions and approvals.</li><li>
Budget and Resource Management:</li><li>
Develop and manage clinical trial budgets, ensuring efficient use of resources and timely financial reporting.</li><li>
Monitor and control trial costs to ensure alignment with project forecasts and company objectives.</li><li>
Negotiate contracts and budgets with clinical vendors and investigators.</li><li>
Vendor and Site Management:</li><li>
Oversee the selection and management of clinical research sites and clinical vendors (CROs, laboratories, etc.) and ensure they meet performance expectations.</li><li>
Develop strong relationships with clinical sites and external partners to ensure aggressive site startup, high-quality data collection and trial conduct.</li><li>
Perform risk assessment and management, addressing issues proactively to mitigate operational issues.</li></ul><p></p><p><b><br>
Qualifications:</b></p><ul><li>
Bachelor's or Master's degree in life sciences or a related field.</li><li>
7+ Years of experience as a Clinical Project Manager for Class II/III device studies</li><li>
3+ years of regulatory/clinical trial experience in the medical device industry</li><li>
Demonstrates working knowledge of clinical trial design</li><li>
Minimum of three years of experience developing clinical documents including protocols, informed consent, clinical study reports, and investigator brochures among other documents.</li><li>
Knowledge of financial principles in budgeting, budget negotiation, &amp; contracts management.</li><li>
Demonstrates data management skills, tracking study metrics, and adherence to study protocol</li><li>
Fluent in English with oral presentation and training capabilities</li><li>
Able and willing to travel as needed, up to 30%</li><li>
Expertise in GCP and regulatory requirements.</li><li>
Strong leadership and team management skills.</li></ul></div><p></p>

Clinical Project Manager

caresoft.pvt.ltd

<p>We are seeking a highly skilled <b>Technical Manager</b> with a strong background in <b>clinical software development</b> and <b>team leadership</b>. The ideal candidate must have <b>6+ years of experience in developing clinical or healthcare applications</b> and have progressed from a <b>developer</b> to a <b>team lead</b> and then into a <b>managerial role</b>. The role requires expertise in <b>core PHP</b>, as our application is built on this technology stack.</p><p><b>Key Responsibilities:</b></p><ul><li>Lead and manage the development team, ensuring the delivery of high-quality clinical software solutions.</li><li>Oversee the entire <b>software development lifecycle (SDLC)</b>, from planning and design to deployment and maintenance.</li><li>Collaborate with <b>healthcare professionals</b> and stakeholders to understand system requirements and ensure compliance with industry standards.</li><li>Optimize and enhance existing <b>PHP-based clinical applications</b> for better performance and security.</li><li>Mentor and guide developers, ensuring best practices in coding, architecture, and database management.</li><li>Implement <b>technical strategies</b>, conduct code reviews, and ensure adherence to coding standards.</li><li>Stay updated with the latest <b>healthcare IT trends</b> and regulatory requirements (HIPAA, HL7, etc.).</li><li>Troubleshoot technical issues and provide <b>scalable solutions</b> for system improvements.</li><li>Manage project timelines, resource allocation, and risk assessment to meet business objectives.</li></ul><p><b>Requirements:</b></p><ul><li><b>6+ years</b> of experience in <b>clinical/healthcare software development</b>.</li><li>Proven experience as a <b>Developer</b>, <b>Team Lead</b>, and <b>Technical Manager</b>.</li><li>Strong expertise in <b>core PHP</b> and experience with <b>MySQL, JavaScript, and related web technologies</b>.</li><li>Hands-on experience with <b>API development, system integrations, and healthcare data management</b>.</li><li>Familiarity with <b>EMR/EHR systems</b>, <b>HL7, FHIR</b>, or other clinical data standards is a plus.</li><li>Strong leadership skills with the ability to mentor and manage a development team.</li><li>Excellent problem-solving abilities and experience in performance optimization.</li><li>Knowledge of <b>agile development methodologies</b>.</li><li>Strong communication skills to work with technical and non-technical stakeholders.</li></ul><p><b>Preferred Qualifications:</b></p><ul><li>Experience with <b>Laravel or other PHP frameworks</b>.</li><li>Understanding of <b>healthcare compliance regulations (HIPAA, GDPR, etc.)</b>.</li><li>Experience in <b>cloud technologies</b> and <b>DevOps practices</b> is a plus.</li></ul><p>Job Type: Full-time</p><p>Pay: Rs270,000.00 - Rs370,000.00 per month</p><p>Application Question(s):</p><ul><li>What is your current salary?</li><li>What is your expected salary?</li><li>have you progressed from a developer to a team lead and then into a managerial role ? Yes/NO</li></ul><p>Experience:</p><ul><li>Core PHP Development: 6 years (Required)</li><li>Clinical software development: 5 years (Preferred)</li><li>International client: 5 years (Preferred)</li></ul><p>Location:</p><ul><li>Rawalpindi Satellite Town (Required)</li></ul><p>Work Location: In person</p>

Technical Manager Core PHP

Emirates Home Nursing

<p>&sect; Adhere to company&rsquo;s vision, mission and core values.</p><p>&sect; Adhere to organizations communication structure and accountabilities.</p><p>&sect; Maintains confidentiality and avert conflict of interest.</p><p>&sect; Accountable for providing and maintaining a good reputation as the face of the company.</p><p>&sect;Representing the agency in all forms and every aspect.</p><p>&sect;Responsible for overseeing the cash flow and financial instruments</p><p>&middot;</p><p>&middot; Provide physiotherapy to patients of all ages</p><p>&middot; Undertake and record a thorough assessment using appropriate techniques and equipment</p><p>&middot; Accompany the Clinical Manager in visiting patients&rsquo; homes to complete assessments as and when required</p><p>&middot; Provide appropriate advice based on the patient&rsquo;s medical, social and cultural circumstances</p><p>&middot; Plan and deliver individual physiotherapy treatment programs</p><p>&middot; Create progress plans with the patients and their family to understand their targets and goals</p><p>&middot; Communicate highly sensitive and complex information in an understandable way to the patient and their family</p><p>&middot; Adapting best practices on the patient care management</p><p>&middot; Provide monthly reports on the cases handled along with the patient&rsquo;s status</p><p>&middot; Participate on developing clinical SOP on the rehabilitation treatment of the patients as per local and international guidelines.</p><p>&middot; Ensure the schedule provided is realistic and can be achieved weekly</p><p>&middot; Complete progress reports and provide to the Clinical Manager on a daily basis</p><p>&middot; Respect patient confidentiality at all times and provide information only within the professional context</p><p>&middot; Manage clinical risk in the homecare setting</p><p><b>Essential Education &amp; Experience</b></p><p>&middot; DHA license &ndash; Physiotherapist</p><p>&middot; Physiotherapy degree or equivalent</p><p>&middot; A minimum of 3 years&rsquo; working experience</p><p><b>Specific Knowledge/ skills</b></p><p>&middot; Good rapport with patients</p><p>&middot; In-depth knowledge of best practices and policies</p><p>&middot; Ability to work well under pressure and in fast paced environment</p><p>&middot; Ensure to be passionate about the role and have a fondness for caring for people</p><p>&middot; Aware of the DHA homecare standards/requirements for Speech therapist services</p><p><b>Care Skills Compassion Customer Service</b></p><p><b>Proactive Individual Adaptability Strong English speaking skills</b></p><p>Job Type: Full-time</p><p>Pay: AED8,000.00 - AED10,000.00 per month</p><p>Experience:</p><ul><li>Speech Therapist: 2 years (Preferred)</li></ul><p>Language:</p><ul><li>Arabic language (Required)</li></ul><p>License/Certification:</p><ul><li>DHA LICENSE- Speech Therapist (Required)</li></ul>

Speech therapist

Novartis

<div><div><h3 class="jobSectionHeader"><b>Summary
</b></h3><div>Job Title: Clinical Sourcing Manager, R&amp;D<br>
#LI-Hybrid<br>
Location: Hyderabad, India<br>
<br>
The Clinical Sourcing Manager generates, negotiates, and executes contracts to support the utilisation of clinical Contract Research Organisations (CROs) for Novartis Clinical Trials. This role assures compliant, high-quality, timely, and cost-effective external service delivery to support the Novartis drug development pipeline. The Clinical Sourcing Manager also participates in projects and initiatives to ensure Clinical Contracting &amp; Outsourcing Management is prepared to respond to changing needs and requirements (legal, operational, regulatory, and financial).</div>
</div><div><h3 class="jobSectionHeader"><b>About the Role
</b></h3><div><p><b>Major accountabilities:
</b></p><ul><li>Prepare and release RFI, RFP, and RFQs; negotiate with suppliers for new requests and scope changes.</li><li>
Act as the main contact with vendors for negotiation of scope of work, study assumptions, pricing, and payment schedules.</li><li>
Negotiate, develop, and execute contract frameworks (including MSAs &amp; SLAs) with key suppliers and ensure implementation.</li><li>
Collaborate with legal, finance, and QA to ensure agreements are commercially advantageous and minimise risk.</li><li>
Select ESPs based on category strategy, value-added services, cost avoidance, and savings opportunities.</li><li>
Drive productivity improvements and ensure spend/contract compliance, including monitoring and reduction of maverick spend.</li><li>
Ensure complete contract packages for clinical ESP activities and secure necessary approvals for compliance.</li><li>
Contribute to vendor audit requests and facilitate corrective action plans.</li><li>
Ensure ESPs deliver in line with expectations and contracts.</li><li>
Proactively identify and pursue new ideas and opportunities to create value.</li></ul><p><b>
Minimum Requirements:
</b><br>
<b>Work Experience:
</b></p><ul><li>Minimum Bachelor&rsquo;s degree in Life Sciences or Pharmaceutical Sciences required.</li><li>
Master&rsquo;s/other advanced degree or MBA in business administration or a scientific field preferred.</li><li>
Minimum 5 years&rsquo; experience in Clinical Development, including clinical trial budget development.</li><li>
Minimum 5 years&rsquo; experience in Outsourcing within Pharma or CRO industry.</li></ul><p></p><p><b>
Languages :</b></p><ul><li>
English.</li></ul></div>
</div><div><div><p><b>Why Novartis:</b> Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture</p><p><b>
Join our Novartis Network:</b> Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network</p><p><b>
Benefits and Rewards:</b> Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards</p></div></div></div>
<br><div><div>Division
<div>Operations
</div></div><div>Business Unit
<div>Universal Hierarchy Node
</div></div><div>Location
<div>India
</div></div><div>Site
<div>Hyderabad (Office)
</div></div><div>Company / Legal Entity
<div>IN10 (FCRS = IN010) Novartis Healthcare Private Limited
</div></div><div>Alternative Location 1
<div>Selangor, Malaysia
</div></div><div>Functional Area
<div>Procurement
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No
</div></div><div>
</div><div><h3 class="jobSectionHeader"><b>Accessibility and accommodation</b></h3><p>
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.</p>
</div><div><p>Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</p></div></div><div></div>

Clinical Sourcing Manager, R&D

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