Role Description Edison Scientific is currently recruiting a Biostatistician Consultant for a flexible, part-time advisory role. In this capacity, you will act as a domain authority, establishing the primary benchmark for AI-driven statistical results to ensure our system delivers outputs that are technically sound, meet regulatory standards, and reflect the latest requirements from governing agencies. This engagement is designed to fit around existing commitments, at approximately 5–20 hours per week. - Knowledge sharing about "day-in-the-life" as an expert working with data in these domains to assemble regulatory submissions. - Describing common tasks or problems where AI could be of value in your workflows. - Identify + describe internal pharma systems that are commonly used for standard workflows. - Generate or review reference ground-truth artifacts to evaluate against - reports, data files, modules, etc. - Identify + add realistic sources of variance or data corruption in study data. - Identify and correct discrepancies in data quality. Qualifications - 10+ years of experience in biostatistical applications within biotech or pharma, preferably at a sponsor. - Graduate degree (Ph.D. preferred) in Statistics, Biostatistics, or a similar discipline. - Proven expertise in crafting SAPs, determining sample sizes, and designing early-phase (I/II) clinical trials. - Deep familiarity with ICH guidelines and FDA regulatory standards, including direct experience with CSRs and IND filings. Benefits - Remote/US based. - Flexible hours / flexible time zone - 5-20 hours per week. - Competitive salary and equity. - Full healthcare coverage — we pay 100% of premiums for you and your dependents. - Support for growing families, including a yearly new parent stipend and fertility coverage through Carrot. - Mental health support through Rula, our in-network therapist and psychiatrist network with fast availability. - 12 weeks of paid parental leave for maternity, paternity, and adoption. - Pet care support with a yearly employer-funded stipend for your animal companions. - Commuter benefits so you can pay for transit and parking with pre-tax dollars. - 401(k) company matching. - $300 health and wellness benefit quarterly. - Lunch is on us every day you're in the office, and dinner is on us when you're working late. - Regular team offsites and company events. - A fast-moving, mission-driven culture where smart people do their best work and actually enjoy doing it.

Role Description Our Research Quality Manager is responsible for implementing the quality assurance program, managing and performing consult/support visits at investigative sites, assisting with onsite external audits and inspections, and providing routine quality support for assigned investigative sites. This is a fully remote position in the US; relocation assistance and visa sponsorship are not available. - Develops and maintains effective relationships with investigative sites and other SCRI departments and colleagues - Monitors and modifies policies and procedures - Utilizes quality tools that assess the quality indicators of study operations - Monitors quality indicators for all sites using Risk-Based approach and within framework of QBD – Quality by Design - and prioritizes quality indicators depending on severity/urgency - Identifies areas of deficiency in quality and reports those deficiencies to SC Directors and other appropriate colleagues - Assists the business in development and modification of process documents - Assists with preparation and hosting of external audits - Assists research staff in maintaining regulatory compliance - Performs process / focused audits (as needed) of research sites utilizing research audit tools to ensure quality and reports audit findings to the appropriate leadership - Ensures timely and appropriate follow-up in areas of deficiency - Communicates observations and deficiencies to the Site Director / Manager and study PI, as appropriate - Assists sites with Root Cause analysis and responses to external audits and CAPAs - Maintains records of audits and reports - Communicates with monitors and auditors of clinical trials, as needed - Educates staff in quality improvement methods and industry trends - Other duties as assigned Qualifications - Bachelor’s Degree required, Master’s Degree preferred - Minimum 3 years’ work experience in Quality Assurance, Quality Management, or Quality Auditing preferably in a clinical research, healthcare or life sciences field - Expertise in GCP, FDA and other applicable regulations in a risk-based environment Benefits - Comprehensive benefits to support physical, mental, and financial well-being - Competitive compensation package determined by performance, experience, skills, equity, and geographical markets - Other compensation, such as an annual bonus or long-term incentive opportunities may be offered Company Description Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.

Role Description As a Senior Clinical Monitoring Lead, you will play a pivotal role in leading the clinical monitoring function within assigned studies to ensure high-quality trial execution and regulatory compliance. You will oversee Site Managers and Clinical Trial Coordinators, ensuring effective monitoring of clinical sites, adherence to ICH-GCP and SOPs, and timely resolution of study issues. Your leadership will support operational readiness for inspections, data integrity, and consistency across all monitoring activities. In larger or complex clinical trials, you may provide operational leadership over Clinical Monitoring Leads, ensuring that all clinical monitoring functions align with the overall project goals. By bringing your expertise and dedication, you will contribute significantly to the success of our clinical trials and the broader business objectives. What You’ll Do - Lead and manage Site Managers in all aspects of site monitoring, including site selection, initiation, routine monitoring, and close-out. - Review monitoring visit reports and follow-up letters for accuracy, completeness, and compliance with protocol, SOPs, and regulatory requirements. - Ensure consistent application of risk-based and centralized monitoring strategies across studies. - Track and report on site performance, enrollment, data quality, and issue resolution. - Ensure timely and accurate documentation in the Trial Master File (TMF) and support audit and inspection readiness. - Partner with Quality Assurance to conduct root cause analyses and implement corrective and preventive actions (CAPAs). - Supervise, coach, and mentor Site Managers, conduct performance reviews, and support professional development. - Deliver training to Site Managers on protocol requirements, therapeutic area knowledge, and monitoring best practices. - Collaborate with CTDU, CTAU, and other stakeholders to align on trial execution operational strategies. - Act as a subject matter expert on monitoring execution for internal and external partners. - Manage all aspects of monitoring operations and quality for allocated studies, ensuring compliance with ICH GCP and applicable local regulations. - Contribute to the development of clinical tools and documents. Qualifications - Bachelor’s degree in life sciences, nursing, pharmacy, or related field; advanced degree preferred. - Minimum of 10 years of clinical research experience, including at least 3 years as a CRA. - Minimum of 5 years in CRA management, mentoring, or monitoring oversight. - Strong understanding of ICH-GCP, FDA/EMA regulations, and global clinical trial guidelines. - Demonstrated experience in CRA performance management and inspection readiness. - Excellent organizational, leadership, and problem-solving skills. - Strong communication skills, both written and verbal. - Willingness to travel (20–30%, as required). - Ability to build relationships across the organization and operate effectively in a hybrid or remote environment. - Proven ability to manage multiple tasks of varying complexity within tight timelines and shifting priorities. - Strong leadership skills with the ability to influence and drive performance across clinical trial teams. Preferred Skills - Advanced degree in life sciences or related field. - Experience with global clinical trial management. - Familiarity with advanced clinical monitoring tools and technologies. Benefits - Medical, Dental, Vision, & Life insurances. - Fitness & Wellness programs including a fitness reimbursement. - Short- and Long-Term Disability insurance. - A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31). - Up to 12 company paid holidays + 3 paid days off for Personal Significance. - 80 hours of sick time per calendar year. - Paid Maternity and Parental Leave benefit. - 401(k) program participation with company matched contributions. - Employee stock purchase plan. - Tuition reimbursement of up to $10,000 per calendar year. - Employee Resource Groups participation.

Role Description This position is for experienced Clinical Research Associates with 1+ years of independent monitoring experience. You will manage clinical trial sites across Germany, ensuring studies are conducted in compliance with the protocol, ICH-GCP, applicable regulations, and company SOPs. You’ll work autonomously, partner closely with investigative sites, and collaborate with project teams to deliver high-quality, inspection-ready clinical trials. What You’ll Do - Perform site monitoring activities (on-site and remote) using a risk-based monitoring approach - Ensure protocol, ICH-GCP, regulatory, and SOP compliance at investigator sites - Conduct SDR, SDV, CRF review, and investigational product accountability - Identify, document, escalate, and follow up on issues through resolution, applying root cause analysis and CAPA principles - Maintain audit and inspection readiness at all assigned sites - Build strong, collaborative relationships with investigators and site staff - Document monitoring activities in timely, high-quality reports and follow-up letters - Maintain ongoing communication with sites between visits to support issue resolution and data quality - Ensure study systems (e.g., CTMS) are updated according to study conventions - Provide trial status updates and metrics to the Clinical Team Manager (CTM) - Support study start-up, investigator identification, site initiation, and study close-out activities as assigned - Participate in investigator meetings, audits, inspections, and project team meetings as required - Additional responsibilities may include supporting process improvement initiatives, mentoring activities, or project-specific tasks aligned with experience. Qualifications - Bachelor’s degree in a life sciences related field or equivalent qualification - Minimum 1+ years of experience as a Clinical Research Associate / Monitor - Valid driver’s license - Full right to work in Germany - Fluency in German and English (C1 level) – interviews will be conducted in German Requirements - Strong clinical monitoring skills with hands-on RBM experience - Excellent understanding and application of ICH-GCP and applicable regulations - Solid therapeutic area knowledge and medical terminology - Well-developed critical thinking, problem-solving, and root cause analysis skills - Strong written and verbal communication skills with medical professionals - High attention to detail and strong organizational skills - Ability to work independently while contributing effectively to cross-functional teams - Flexibility and adaptability in a dynamic project environment - Proficiency in Microsoft Office and ability to learn clinical systems (e.g., CTMS) Benefits - Competitive salary - Extensive benefits package focused on health and well-being - Flexible working culture that values work-life balance - Award-winning learning and development programme Company Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Through our PPD® clinical research services, we support clinical trials in more than 100 countries, delivering laboratory, digital and decentralized solutions that help bring life-changing therapies to patients faster. Our goal-driven teams combine and deliver startup activities for the clinical trials, collaborating to improve processes, cycle and flexibility. We partner with our sites, businesses and colleagues around the world to decrease startup timelines and exceed expectations.