Title: Part -Time Clinical Registered Dietitian (Hybrid – 75% Remote) Location: Yonkers, New York, 10701, United States Department: Health Care Job Information Work Experience 1-3 years Industry Health Care Salary $40.00-$45.00/hr City Yonkers State/Province New York Zip/Postal Code 10701 Job Description Part-Time Clinical Registered Dietitian (Hybrid – 75% Remote) New York (Local Travel Required) RD Nutrition Consultants LLC is seeking a Part-Time Clinical Registered Dietitian to provide nutrition services to nine group home programs in New York. Join RD Nutrition Consultants LLC and become part of a team that values flexibility, autonomy, and meaningful clinical impact. This position is ideal for a Registered Dietitian looking for consistent part-time hours with a combination of short onsite visits and remote work. Position Details - Hours: 5–8 hours per week - Schedule: Flexible - Work Type: Approximately 75% remote - Compensation: $40.00–$45.00 per hour (based on experience) - Travel Time: Compensated at the same hourly rate - Mileage Reimbursement: Provided - Service Area: Nine group homes in New York - Work Setting: - Short monthly onsite visits - Documentation, care planning, and administrative responsibilities may be completed remotely Responsibilities - Conduct comprehensive nutrition assessments and develop individualized nutrition care plans. - Monitor residents' nutritional status and provide follow-up recommendations as appropriate. - Provide nutrition education and counseling to residents, caregivers, and staff. - Collaborate with interdisciplinary team members to support resident health and wellness. - Participate in quality improvement initiatives to promote optimal nutrition outcomes. - Review menus and provide recommendations to ensure nutritional adequacy and regulatory compliance. - Conduct kitchen sanitation reviews and provide recommendations for improvement as needed. - Maintain timely and accurate documentation. - Adhere to all facility policies, procedures, and applicable regulatory requirements. - Perform additional duties as assigned and within the Registered Dietitian scope of practice. Experience & Qualifications - Bachelor's or Master's degree in Dietetics, Nutrition, or a related field from an accredited program. - Registered Dietitian credential through the Commission on Dietetic Registration (CDR). - Minimum of one year of clinical experience preferred. - Experience working with individuals with autism spectrum disorder and/or intellectual and developmental disabilities is strongly preferred. - Strong communication and interpersonal skills. - Ability to work independently while collaborating effectively with interdisciplinary teams. - Proficiency in clinical nutrition assessment and documentation. - Familiarity with state survey processes and nutrition care regulations is preferred.

Role Description Reporting to the Head of Biometrics, this individual will contribute to daily statistical activities and support the development of statistical approaches for clinical trials. Working closely with internal and external stakeholders, you will help manage a growing portfolio of trials. This role also offers the opportunity to support the continued growth of the biostatistics function at Entrada and gain valuable experience in a collaborative, fast-paced environment. Responsibilities - Support statistical strategy for assigned drug programs, including input to clinical development plans, clinical study concepts and protocols design, SAPs, clinical study reports, regulatory documentation and associated publications. - Accountable for oversight of the production of biostatistics deliverables (TFLs, including planned, post-hoc, and/or exploratory analyses) as performed by external resources. - Provide statistical strategy support and input in protocols, CSRs, and scientific presentations and manuscripts. - Review the randomization procedures and oversight of the production of randomization lists. - Review study Case Report Forms, data management plan and other data management related documentation to ensure that specific statistical requirements defined in the study protocol are met. - Oversee outsourced statistical CRO activities and deliverables, ensuring high quality and timely delivery. - Produce innovative tools and methodologies for statistical analysis through literature review. - Participate in the development of department strategies and cross functional initiatives on standards, infrastructure, and processes. Qualifications - Ph.D. in Statistics or a related field, with 6+ years of experience in statistical analysis within the biotech/pharmaceutical industry. - Experience with a broad array of statistical approaches and experience in proposing novel approaches to support acceleration of clinical programs. - Knowledge in the latest developments in the analytical world including machine learning and artificial intelligence is a plus. - Solid understanding of regulatory guidelines on drug development, regulatory submissions, and statistical practice. - Strong statistical programming skills (R, SAS, Python). - Understanding of regulatory guidelines related to submission of datasets using CDISC, development of SDTM and ADaM specifications. - Strong vendor management experience. - Previous experience in Neuromuscular, Ophthalmology or related TA is preferred. - Excellent verbal and written communication skills, coupled with strong attention to detail and proactive mindset. Requirements - This is a US based remote position, with preference given to local New England based candidates. - This role will require a minimum quarterly travel to the Entrada Therapeutics Headquarters located in Boston, MA. Benefits - Comprehensive health, dental and vision coverage. - Life and disability insurance. - 401(k) match. - Paid, gender-inclusive parental leave. - Holistic support for health and well-being. - Education reimbursement. - Discretionary time off. - Commuting benefits aligned to your working model.

• Perform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings. • Perform project management activities for identified projects including resource planning, timelines, and milestone management. • Preparation of Statistical Analysis Plans (including mock TFL shells) for medium complexity studies under the supervision of more senior statistical staff. • Perform complex statistical analyses, quality check statistical analyses developed by other statisticians. • Conduct overall statistical review of TFLs for complex studies prior to client delivery. • Review CRF and other study specific specifications and plans. • May perform sample size calculation for simple studies under the supervision of more senior statistical staff. • Develop the statistical sections of the protocol for simple to medium complexity studies under the supervision of a statistical consultant. • Provide statistical input and review of the CSR for medium complexity studies. • Preparation and review of randomization specifications and generation of randomization schedules. • Mentor of biostatisticians within project activities; assigned tasks related to the development of staff within the department. • Present and share knowledge at team meetings and/or at monthly seminars. • Attend bid defense meetings for medium complexity studies in order to win new business. • Represent the department during project-driven client audits. • All other duties as needed or assigned.

Role Description As a Clinical Consulting Pharmacist, you will: - Provide clinical review and consultation on medication requests, prior authorizations, and benefit determinations. - Evaluate therapy appropriateness, dosing, and safety based on evidence-based guidelines. - Collaborate with providers to clarify prescriptions and recommend alternatives when appropriate. - Support complex case reviews and appeals with accurate clinical documentation. - Identify opportunities to improve medication adherence, safety, and cost-effectiveness. - Educate internal teams on formulary management, utilization review, and pharmacy policy updates. Qualifications - R.Ph required; PharmD preferred. - Full, current, and unrestricted pharmacist license in PA, TN, and/or OH. - Ability to obtain additional state licensure based on business needs. - 1+ year of pharmacy experience preferred (retail, hospital, or managed care). - Working knowledge of formulary management, clinical guidelines, and pharmacy benefit structures. - Strong communication, analytical, and consultative skills. - Ability to exercise sound clinical judgment and work independently. - Commitment to evidence-based practice and continuous learning. Benefits - Competitive Pay $115-$120K annual salary + $5,000 sign-on bonus with shift differential. - Comprehensive Benefits Package (Health, Dental, Vision, PTO, Sick Time, 401k w/match, etc.). - Growth Opportunity and Career Advancement. - Agile and Adaptable team culture. - Innovative and revolutionary technology solutions. - A higher calling to provide quality patient care.