• You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct. • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Title: Senior Clinical Research Associate Location: Melbourne Australia Part time Job requisition id JR 9344 Job Description: For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. About the Role We are seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join our team on a 0.2 FTE (one day per week equivalent) basis. This is an excellent opportunity for an experienced CRA looking for flexible, part-time work while contributing to high-quality clinical research projects. Key Responsibilities - Conduct site monitoring visits (remote and on-site as required) in accordance with study protocols, ICH-GCP, and regulatory requirements - Ensure data integrity and compliance through source data verification (SDV) - Build and maintain strong relationships with investigational sites - Support site initiation, monitoring, and close-out activities - Identify and escalate risks or issues impacting study delivery - Assist with regulatory document review and maintenance of Trial Master Files (TMF) - Collaborate with cross-functional teams to ensure smooth study execution About You - Previous experience as a Clinical Research Associate (or similar role) - Strong understanding of ICH-GCP guidelines and clinical trial processes - Excellent communication and organisational skills - Ability to work independently with minimal supervision - Located in NSW or Melbourne, with willingness to travel occasionally if required - Relevant degree in life sciences, nursing, or a related field preferred We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office. - ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*

Title: Supervisor, MSRDP Location: Dallas United States Job Description: Location: Dallas, TX Location Type: Hybrid Job Number: 937926 Category: Insurance/Billing WHY UT SOUTHWESTERN? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report(Opens in a new window), we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more. We invite you to be a part of the UT Southwestern team where you’ll discover a culture of teamwork, professionalism, and a rewarding career! JOB SUMMARY This position is responsible for supervising day-to-day operations of assigned billing group. The successful applicant will manage several direct reports and indirect reports. The successful candidate will oversee a team of technical denial follow-up analysts (6-15 employees) to ensure accurate claims processing, timely payments, and compliance with regulations like HIPAA. Key responsibilities include the following: - Supervising staff - Reviewing invoices/claims - Monitoring accounts receivable - Resolving escalated issues - Tracking key metrics - Training team members on billing systems and regulatory changes Shift: 8-hour flex shift, Monday through Friday Work From Home (WFH): This is a WFH position. The applicant must live within the Greater DFW area. Additional details shall be discussed during the interview. Core responsibilities - Supervision: Lead and manage a team of collections staff to ensure efficient workflow, productivity, and adherence to goals. - Process management: Oversee the day-to-day operations of insurance follow-up and denials management. - Quality assurance: Conduct audits and review insurance claims and patient invoices for accuracy and completeness. - Problem-solving: Resolve complex or escalated billing issues with patients and payers and rectify inefficiencies. - Performance monitoring: Track key revenue cycle metrics, prepare performance reports, and implement strategies to reduce outstanding balances. - Training and development: Train staff on day-to-day processes - Compliance: Ensure the team adheres to all relevant laws and regulations, including HIPAA, payer guidelines, and state and federal rules. - Collaboration: Work with other departments, such as finance and clinical staff, to improve overall revenue cycle processes. BENEFITS UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include: - PPO medical plan, available day one at no cost for full-time employee-only coverage - 100% coverage for preventive healthcare-no copay - Paid Time Off, available day one - Retirement Programs through the Teacher Retirement System of Texas (TRS) - Paid Parental Leave Benefit - Wellness programs - Tuition Reimbursement - Public Service Loan Forgiveness (PSLF) Qualified Employer - Learn more about these and other UTSW employee benefits!(Opens in a new window) EXPERIENCE AND EDUCATION Required - Education High School Diploma or equivalent. - Experience 5 years Experience working with medical claims recovery and/or denials management and regulations within a healthcare or insurance environment. and Preferred - Experience 5 years in a lead or supervisory experience JOB DUTIES - Supervises day-to-day operations of assigned group. - Ensures production and quality control standards are met by reviewing management reports. - Assigns workload to meet production requirements by evaluating production reports. - Maintains performance standards by counseling employees, performing appraisals and providing required training. - Ensures departmental policies and procedure are followed. In addition, develops and revises policies and procedures as needed. Maintains written procedures for workflow by writing or updating procedures as needed. Communicates and educates all applicable information to appropriate personnel and affiliated facilities as required. - Completes reporting to management. - Compiles analyzes, report status and issues involving all aspects of assigned area. Makes recommendations to management to reflect changes by reviewing various reports and other data, identifies conflicts and write resolutions. - Participates in project groups and task force teams. - Completes special projects as assigned by management. - Reviews and analyses information, identifies problems, recommends solutions and/or writes reports for management or other personnel within established performance guidelines. Provides training and makes effective business presentations to staff. - Monitors correspondence received from various. Audits mail returned for bad addresses and updates addresses as needed. Audits patient accounts for mailing problems. - Resolves complex problems and questions by contacting insurance companies, places of employment, or federal agencies. - Performs other duties as assigned. SECURITY AND EEO STATEMENT Security This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information. EEO UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.

• 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 • Manage assigned operational aspects for implementation at investigator sites • Serve as the primary point of contact for assigned investigator sites • Provide protocol training and address protocol related questions from the investigator site staff when required • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities • Collaborate with the Drug Safety Unit and follow-up with investigator sites regarding adverse events • Submit required reports and documentation within required timeframes • Identify and resolve investigator site issues within required timeframes