21-40 of 44 results
Sort By


Pharmaceutical client in NYC hiring two Clinical Research Study Managers for their Global Trials The Clinical Research Study Leader (CRSL) will provide leadership to global Study Management Teams responsible for delivering First in Man, Proof of Concept through to Phase 3 registration studies in various indications. The CRSL will manage a number of studies, either for a single indication or across different indications. The CRSL is accountable for the strategic and tactical study activities,....


Three Medical Directors needed The Medical Director is a board-certified physician who has a history of clinical practice, and has significant experience in the cardio therapeutic area, Endocrinology or Renal, Nephrology therapeutic areas. The Medical Director is knowledgeable of the actions of regulatory bodies, in particular FDA, and has experience in clinical trials. An ideal candidate should have significant experience in renal cardio disease management and would thrive on proactively....


Top Tier Pharmaceutical Company hiring Endocrinologist Field Physician or Senior Field Physician Endocrinology and Diabetes A Field Physician/Sr. Field Physician US Medical Affairs, is a board-certified endocrinologist who has a history of clinical practice, who has significant experience in the therapeutic area of endocrinology and secondary prevention. They will have solid peer relationships with key opinion leaders in their therapeutic area (TA). An ideal candidate should have significant....


Top Tier Pharmaceutical Company hiring Cardiologist Field Physician or Senior Field Physician Cardiology A Field Physician/Sr. Field Physician US Medical Affairs, is a board-certified cardiologist who has a history of clinical practice, who has significant experience in the therapeutic area of cardiology and secondary prevention. They will have solid peer relationships with key opinion leaders in their therapeutic area (TA). An ideal candidate should have significant experience in their....


The Clinical Operation Lead is responsible for developing operational strategy for one or more clinical studies, and leading the cross-functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of studies keeping the....


The Director/Sr. Director of Clinical Development Operations is responsible for clinical operations planning, oversight and execution of multiple studies within one or more clinical development programs. Strategic development and coordination of operational approaches, guiding study level staff, and optimizing vendor performance. Sophisticated internal (cross functional team members) and external (KOLs, site staff) stakeholder communication and interface. Manage and/or mentor Clinical Trial....

- Albany, NY

Automation Engineer Summary: Responsible for designing, developing, implementing, and maintenance of industrial computerized process control and process monitoring systems in a biopharmaceutical manufacturing cGMP environment. Essential Duties and Responsibilities include, but are not limited to the following: - Provide technical automation support and troubleshooting to Manufacturing, Quality Control, and Facilities according to established SOPs and departmental practices. - Perform....


Principal Automation Engineer Reports to: Automation Manager Summary: Performs advanced technical planning, system integration, maintenance, verification, and validation of PLC and HMI based automated process control systems and process monitoring systems in a biopharmaceutical manufacturing cGMP environment. The Principal Engineer is the site Subject Matter Expert on automated process control and monitoring systems for their area of responsibility and is recognized as a technical expert by....


Require a highly motivated and experienced individual for the position of Sr. QA Associate II. This individual will be part of the External Commercial QA group. Responsibilities include supporting Supplier Quality Management activities. Performs vendor audits, supports changes, complaints and queries related to external vendors. Troubleshoots issues, develops and implements effective risk mitigation strategies as required. Collaborates with site operations to insure site expectations of....


POSITION SUMMARY: Seeking an engineer to lead projects in support of small molecule clinical and commercial manufacturing processes. The individual will design, develop, scale-up and optimize robust drug product unit operations that provide high product quality at various scales ranging from R&D to cGMP manufacture. Strong collaboration is expected with internal early R&D groups, internal commercial partners, and external third party CMOs. The candidate should have strong communication


Principal Scientist GLOBAL PHARMACEUTICAL COMPANY is hiring a Technical lead to design and execute analytical related aspects of pharmaceutical drug product development. Has broad and in-depth understanding of analytical techniques to support testing of a range of small molecules and macromolecules. Understanding of biomolecules and bioanalytical techniques including test methods to support clinical studies such as pharmacokinetics studies is desirable. Has method development/validation....

- New York, NY

Head of Gene Therapy CMC My client is expanding and looking to bring on a new person to lead CMC for Gene Therapy. The ideal candidate will take on the following tasks:Plan, lead and communicate the CMC related strategies for gene therapy products, including selecting CROs and CMOs.Actively manage CRO/CMOs for process optimization, scalable cGMP manufacture (both Drug Substance and Product) to supply a multi-product portfolio of pre-clinical and clinical gene therapy development....


Pharmaceutical company in need of Director or Senior Director to join the Medical Affairs team. The Medical Director will provide support and expertise in the area of psychiatry either Schizo or Addiction as there are two needs In this newly created and high profile role you will serve as the medical affairs strategic lead for our combination oral schizophrenia treatment that is currently in phase 3 clinical development. The Medical Director is expected to establish key medical strategies for....


The Lead, Human Factors Engineering will be serve as a local leader for the Human Factors Engineering Team as it grows. This role will lead human factors work to support the development of devices and combination products for delivery of our wide portfolio of drugs and biologics. This includes leadership in human factors planning, use-related risk management, requirements development and execution of human factors research (user research, formative and summative studies).1. Responsible for....

- Menlo Park, CA

Education and Qualifications - Pharm.D., PhD, or M.D. or equivalent education. - Preferable five to seven years clinical or clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry. - Participated in clinical oncology studies. Overview The Medical Director will collaborate with company management, design, plan and develop clinical evaluation research studies in hematology oncology. He / She will prepare, author and maintain....


Device Development Leader is high impact position for leading development of product device strategy, including technology/platform choice, partner/vendor selection, clinical strategy, regulatory strategy. Requires talented leader with proven expertise in overseeing cross-functional global team activities and to be knowledgeable about overall device development activities. As leader of device development subteam, accountable for device program execution ensuring the translation of product....


The primary objective of the Associate Director, Employee Communications is to partner with the Talent Management leader and team, Human Resources team and managers/leaders across the organization to bring company’s mission and values to life for employees to help drive results, increase enterprise value and assist in attracting & retaining talent. The position will play a role in developing and delivering an employee communication strategy for the global organization. This role will....


Reporting the US Head of Oncology Medical Affairs this Solid Tumor Lead will be accountable for the development and execution of the US Solid Tumor medical affairs strategy. Through cross-functional leadership and deep understanding of the treatment landscape, the Platform Lead will provide oversight and strategic direction to a team of US Medical Leads in development and execution of US medical plans including external engagement, communication and evidence generation strategies and....


Act as recipe lead on DeltaV/Syncade driven fully integrated facility startup, reporting into global Execution Systems organization. Create DeltaV and Syncade design and recipe standards for project that will be used as global standards. Requires extensive experience and strong knowledge of DeltaV and ISA-S88 standards. Strong communication and interpersonal skills. Responsible for the technical setup and structure of the DCS system (DeltaV) and MES system (Syncade) to enable the Start-up,....


The Senior Manager Clinical Operations is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Senior Manager Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of

21-40 of 44 results

Let's get your search started.

Contact Us