Associate Director, Clinical Operations Salary at Patheon By Thermo Fisher Scientific BETA

Job Title: Project Manager Location: Durham, NC Reports to: Director, Project Management On-Site Expectations: Onsite About MedPharm: MedPharm is a global leader in topical and transdermal product development, providing end-to-end services from early-stage formulation development to full commercial production. With facilities in the UK and the US, MedPharm has established itself as a trusted partner in dermatological, nail, mucosal, respiratory, and transdermal drug delivery. MedPharm has a strong track record of supporting product development and pioneering performance testing models to reduce development risks for its clients. Job Purpose: The Project Manager plays a critical role in leading and executing client programs across MedPharm’s end-to-end CDMO services. This client-facing position ensures seamless project execution by coordinating internal teams, managing key project milestones, and driving revenue through proactive scope management. Acting as the primary liaison between c

Overview: Lead and perform Quality Assurance (QA) initiatives and duties at PharPoint Research, including all project and non-project activities performed. Responsible for assisting with the creation and implementation of quality initiatives at the company, including but not limited to: Standard Operating Procedures (SOPs) and training, computer systems validation (CSV), and Quality Management System (QMS). What you will do: Provide consultation and assist with decisions as it relates to the company and departmental QA strategy and departmental goals. Generate, approve and implement external and internal audit plans and processes. Organize and conduct internal audits in accordance with the internal audit schedule. Coordinate and host sponsor audits; manage and implement responses to audit observations. Plan, schedule, conduct and report investigator site audits, Trial Master File (TMF) audits and vendor audits. Coordinate and assist in regulatory inspections; assist with coordinating a

Who we are We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive enviro

We are seeking a Senior Director and General Manager of Genomics to join IQVIA Laboratories in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Senior Director and General Manager of Genomics holds accountability for driving global profitability and expansion of the Genomics business. The ideal candidate should possess relationship-building skills, strategic thinking abilities, a visionary mindset, scientific acumen, preclinical and clinical trial experience to elevate the business to new heights. Job Description Manage Global Genomics business to ensure profitability and the delivery of quality products and services to clients. Work closely with go-to-market teams to identify and assess potential opportunities ensuring a robust pipeline of new and existing business. Contribute to the developmen

Fortrea's FSP team is hiring experienced Sr. Project Managers! Seeking current Sr. PMs with experience working for a Sponsor directly or within a FSP model. Oncology experience preferred. Home Based in the US. Job Overview: At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met. The Senior Project Manager is expected to have a working knowledge of drug development and clinical trial execution. They also compile and drive documentation for the project, ensuring the accuracy and quality of regulatory data. The Senior Project Manager may also have line management and / or business development responsibilities. Summary of Responsibiliti

Senior Scientist (Durham, NC, USA) – Join a Growing Biotech Company! The Senior Scientist is part of the Product Development team at LaCAR US, Inc., responsible for assay development projects to add new assays to the growing portfolio of test solutions offered in the Newborn Screening business. The Scientist will lead and perform studies focused on the development and optimization of new enzymatic assays, clinical chemistry assays and immunoassays. The Scientist will directly report to the Senior Director, Newborn Screening. Your Key Responsibilities: · Lead development of new enzymatic assays, clinical chemistry assays (enzyme, substrate and general chemistry) and immunoassays on the digital microfluidic platform. · Optimize assay design and reagent formulations using DOE tools to achieve desired levels of performance and stability. · Characterize assay performance across various analytical performance metrics including precision, specificity and sensitivity. · Derive solutions for te

Job Type Part-time Description Job title Case Manager /Intensive Case Manager Reports to Program Director Position Summary The case manager will determine resources needed to meet the individualized needs of the participant. The case manager will take all necessary actions in assuring the implementation of the service treatment plan including serving as an advocate for the participant to enable him/her to receive needed services; identification of program needs, service gaps and recommending strategies. A commitment to the RHD values should be demonstrated as job duties are performed. Essential Duties and Functions Team-Based Planning Act as part of a multidisciplinary team designed to provide services from a holistic and Values based perspective. Assist in the development of recovery plans and reviews in collaboration with the program participant, clinical and medical staff and other stakeholders as determined in collaboration with program participant. Develop and maintain relationshi

Are you looking for a position where you can have fun, where you can shine, flourish, learn, and be surrounded by other like-minded professionals?If Yes, then we may be the place for you!Therapy Smarts, Inc is looking to hire dedicated and innovative Senior Board Certified Behavior Analyst (BCBA) to join our growing team in a full-time capacity.Our mission: Turning challenges into triumphs one child at a time.About Us: Therapy Smarts, Inc is a therapist owned private pediatric outpatient clinic providing SLP, PT, OT , Psychological evaluations, and ABA services to children of all ages and diagnoses in the Raleigh-Durham area. At Therapy Smarts we pride ourselves on our collaborative approach to therapy, drawing upon evidence based and functional training of skills in order to improve the quality of life of those we serve.Qualities that fit this opportunityMinimum of 3 years experience in the field of ABA including comprehensive intervention development and implementation for children a