Current jobs related to Associate Director, Clinical Sciences - East Hanover - Legend Biotech USA
-
Associate Director, Clinical Sciences
2 days ago
East Hanover, United States Novartis Farmacéutica Full timeChoose LocationChoose Location### Summary#LI-Hybrid Novartis has an incredible opportunity for a talented individual to join our team as an Associate Director, Clinical Sciences. As the Associate Director, Clinical Sciences, you will support US efforts in the planning, execution and reporting of Innovative Medicine US (IM US) clinical trials This position...
-
Associate Director, Clinical Sciences
2 days ago
East Hanover, United States Novartis Group Companies Full timeJob Description Summary #LI-Hybrid Novartis has an incredible opportunity for a talented individual to join our team as an Associate Director, Clinical Sciences. As the Associate Director, Clinical Sciences, you will support US efforts in the planning, execution and reporting of Innovative Medicine US (IM US) clinical trials. This position will be located at...
-
Associate Director, Clinical Sciences
2 days ago
East Hanover, United States Healthcare Businesswomen’s Association Full timeJob Description Summary Job Description Summary - Novartis has an incredible opportunity for a talented individual to join our team as an Associate Director, Clinical Sciences. As the Associate Director, Clinical Sciences, you will support US efforts in the planning, execution and reporting of Innovative Medicine US (IM US) clinical trials. This position...
-
Associate Director, Clinical Sciences
2 days ago
East Hanover, United States Novartis Group Companies Full timeJob Description Summary #LI-Hybrid Novartis has an incredible opportunity for a talented individual to join our team as an Associate Director, Clinical Sciences. As the Associate Director, Clinical Sciences, you will support US efforts in the planning, execution and reporting of Innovative Medicine US (IM US) clinical trials This position will be located at...
-
Associate Director, Clinical Sciences
2 days ago
East Hanover, United States Novartis Full timeOverview Summary Novartis has an incredible opportunity for a talented individual to join our team as an Associate Director, Clinical Sciences. As the Associate Director, Clinical Sciences, you will support US efforts in the planning, execution and reporting of Innovative Medicine US (IM US) clinical trials. This position will be located at the East Hanover...
-
Associate Director, Clinical Trials
2 days ago
East Hanover, United States Novartis Farmacéutica Full timeA global pharmaceutical company is seeking an Associate Director, Clinical Sciences in East Hanover, NJ. This role involves leading clinical trials, managing relationships with stakeholders, and mentoring team members. Candidates should have a minimum of 8 years of relevant experience and a strong understanding of FDA guidelines. The position offers a...
-
East Hanover, United States Novartis Group Companies Full timeA leading pharmaceutical company is seeking an Associate Director of Clinical Sciences in East Hanover, NJ. You'll implement clinical trials, mentor associates, and ensure compliance with FDA guidelines. This role requires substantial clinical research experience and strong communication skills. A comprehensive benefits package and competitive salary range...
-
Director, Clinical Sciences, Therapeutic Lead
3 weeks ago
East Hanover, United States Novartis Full timedivh2Director, Clinical Sciences, Therapeutic Lead/h2pNovartis has an incredible opportunity for a talented individual to join our team as a Director, Clinical Sciences, Therapeutic Lead. As the Director, Clinical Sciences, Therapeutic Lead, you will support US efforts in the planning, implementation, execution, and reporting of US Medical Affairs assigned...
-
Director, Clinical Sciences, Therapeutic Lead
4 weeks ago
East Hanover, United States Novartis Group Companies Full timeJob Description Summary #LI-Hybrid Novartis has an incredible opportunity for a talented individual to join our team as a Director, Clinical Sciences, Therapeutic Lead. As the Director, Clinical Sciences, Therapeutic Lead you will support U.S. efforts in the planning, implementation, execution and reporting of U.S. Medical Affairs assigned therapeutic...
-
Associate Director, Decision Science
1 week ago
East Hanover, United States Novartis Full timeAssociate Director, Decision Science (1 of 2) Join to apply for the Associate Director, Decision Science (1 of 2) role at Novartis Associate Director, Decision Science (1 of 2) 1 day ago Be among the first 25 applicants Join to apply for the Associate Director, Decision Science (1 of 2) role at Novartis Get AI-powered advice on this job and more exclusive...
Associate Director, Clinical Sciences
2 days ago
Job Description Summary
Job Description
Summary Novartis has an incredible opportunity for a talented individual to join our team as an Associate Director, Clinical Sciences. As the Associate Director, Clinical Sciences, you will support US efforts in the planning, execution and reporting of Innovative Medicine US (IM US) clinical trials. This position will be located at the East Hanover site and will not have the ability to be located remotely. This position will require 25% travel as defined by the business (domestic and/ or international). Responsibilities Responsible for the implementation of designated clinical trials including investigator selection, patient recruitment, preparation of trial related documentation, TMF maintenance, and organizing Ethics Committee submissions. May provide strategic input to protocol design based on operational feasibility and execution strategy as appropriate. Accountable for the accuracy and timeliness of trial information in all trial databases and tracking systems. Serves as clinical trial leader for US Medical Affairs Trials (including Phase I-IV, Managed Access, Investigator Initiated, Research Collaborations and Registries). May serve as disease area(s) lead in support of Therapeutic Area Program Lead, Clinical Sciences. Interfaces with the disease area(s), global and US clinical team members, clinical operations, scientific operations, regulatory affairs, drug supply, data management, finance, quality, compliance, and other relevant functional areas. Liaises with study investigators, site research staff, and field-based colleagues to support clinical studies. Point of first contact when investigators/site personnel enquire about patient inclusion/exclusion criteria for ongoing trials. Organizes investigators start-up meeting and study site initiation meetings. Drives study enrollment, plan advisory boards, and perform external study feasibility with investigators. May independently develop strategic trial execution plan (e.g., recruitment retention, contingency plans) and timeline commitments for the US as appropriate. Maintains project files including: ethics committee approvals; curricula vitae of investigators and study personnel; clinical investigators brochure; protocols; case report forms instructions; consent documents; clinical trial material shipping orders; start-up meeting attendance documentation; letters of agreement; lab reference ranges; all investigator and site correspondence; and schedules of payment. Understands and complies with company SOPs and GCPs; contributes to continuous improvement in SOPs and local Working Practices. Responsible for the initial and subsequent drug supply across trials within a therapeutic area in collaboration with the Local Drug Supply Manager. Contributes to the preparation and review of clinical program documents (PowerPoint presentations, IND annual report, Health Authority briefing books, clinical study protocol, regulatory documents, clinical study reports, CSR and submissions) and other study related documents assuring quality and consistency. Supports the development, management and tracking of trial budgets working closely with the appropriate partners. Facilitates vendor selection and performance. Manages all vendors (CRO, Central lab etc.): definition of responsibilities, communication plan, divisions of responsibility, milestones, review monthly status reports, and the interactive management of all vendors to ensure project success. Coordinates the movement of laboratory samples and the resulting data when central laboratory facilities are used. Reviews all SAEs, ensures Medical Director sign-off, that sites are notified, and that all company procedures are complied with. Supports all scientific aspects of clinical trial(s) and program level activities as assigned. Provides mentorship to Managers and Specialists, Clinical Sciences, to ensure that their role and contribution is optimized. Essential Requirements Bachelor's degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institution. A minimum of 8 years of significant clinical research or research monitoring experience that provides the required knowledge, skills and abilities and experience mentoring or training others. In some cases, an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered. Excellent understanding and demonstrated application of FDA guidelines, Good Clinical Practices, and applicable Standard Operating Procedures. Ability to mentor and train other clinical associates in a positive and effective manner. Ability to evaluate medical research data and proficient knowledge of medical terminology. Effective oral and written communication skills, with the ability to communicate effectively with medical personnel. Effective presentation skills. Effective organizational and time management skills. Ability to utilize problem-solving techniques applicable to constantly changing environment. The salary for this position is expected to range between $152,600 and $283,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people, click here. EEO Statement The Novartis Group of Companies are
Equal Opportunity Employer
s. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range $152,600.00 - $283,400 Skills Desired Clinical Monitoring, Clinical Research, Clinical Trial Protocol, Clinical Trials, Decision Making Skills, Drug Development, Health Sciences, Lifesciences, Medical Strategy, Regulatory Compliance #J-18808-Ljbffr
