Collecting information
Organizing data
Creates key business reports as requested by the executive management team related to new business leads, pipeline progression, bookings, open orders, delivery dates, revenue, and accounts payable. Performs other duties as assigned by the executive management team. Experience in healthcare/medical d
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. Per standardized clinical protocols, independently provides and documents clinical
Jobboard is seeking an Associate Director of Regulatory Affairs to provide regulatory support for medical device systems at our San Diego site. The ideal candidate will have over 10 years of experience in the Medical Device industry and at least 5 years in Regulatory Affairs. This role involves deve
Advanced knowledge of medical terminology; experience with data entry and clinical computer systems. Under general supervision of a licensed practitioner and/or department leader, the Clin-Med Assist I independently provides and documents clinical care and associated tasks as assigned and as per sta
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. Per standardized clinical protocols, independently provides and documents clinical
Under general supervision, the Clinical Pharmacist participates as an instrumental member of the healthcare team, working closely with physicians, residents, fellows and nurses to ensure safe, effective, rational and most cost-effective use of medications to the inpatient and clinic pediatric popula
Advanced knowledge of medical terminology; experience with data entry and clinical computer systems. Under general supervision of a licensed practitioner and/or department leader, the Clin-Med Assist I independently provides and documents clinical care and associated tasks as assigned and as per sta
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. Per standardized clinical protocols, independently provides and documents clinical
Under the general supervision of a licensed care provider and/or management, the Clinical Medical Assistant I (CMA I)/ Patient Access Representative II (PAR II) is responsible to function as both a CMA I and a PAR II. Per standardized clinical protocols, independently provides and documents clinical
Clinical advancementUses systematic planning, appropriate methods and timely exchange of information with multidisciplinary team and patient/family to coordinate care. Clinical judgment and decision makingUtilizes the nursing process and a critical thinking approach to provide patient care that inco
The Executive Director, Regulatory Strategy Endocrinology is a senior regulatory leader responsible for shaping and driving global regulatory strategy across Company's Endocrinology pipeline, spanning early development through commercialization. Partners closely with Clinical Development, Safety, C
Vice President, Regulatory Affairs, Clinical Operations & Medical Affairs. The Company is in search of a Vice President for Regulatory Affairs, Clinical Operations, and Medical Affairs. A minimum of 10 years' in regulatory affairs leadership is required, along with significant experience in overseei
The successful candidate will serve as a key medical leader, partnering closely with Clinical Operations, Regulatory Affairs, Biostatistics, Drug Safety, Translational Medicine, Research, and Medical Affairs to advance innovative therapies through development. We are seeking an experienced and strat
Under general supervision, the Clinical Pharmacist participates as an instrumental member of the healthcare team, working closely with physicians, residents, fellows and nurses to ensure safe, effective, rational and most cost-effective use of medications to the inpatient and clinic pediatric popula
Specific responsibilities will include: being the clinical or program lead for the development of clinical research strategies, clinical development plans, and independent direction of Phase 1-4 clinical studies collaboratively within cross-functional project teams (including clinical operations, pr
To qualify for the Regulatory Affairs Specialist III role, candidates must have a Bachelor's degree in life sciences, engineering, or a related field, along with at least 6 years of experience in a regulated environment, including 4 years of direct experience in Regulatory Affairs. Collaborate with
Join our team as a Project Manager in Regulatory Affairs, focusing on Clinical and CMC. Project Management Tools | Regulatory/Document Systems | Collaboration Tools | AI Tools. Project Manager, Regulatory Affairs (Clinical and CMC).
The ideal candidate will have prior experience as a medical monitor on Phase I-IV clinical trials in a pharmaceutical, biotechnology, or CRO setting, and possess a strong knowledge of clinical trial methodology, safety assessment, and medical data review. The successful candidate will be responsible
Some knowledge of clinical drug development process including working knowledge of ICH, Good Clinical Practices (GCPs), FDA regulations, and EU Directive. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and me
The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position (although some travel is required) who will oversee multiple aspects of clinical trial conduct including study start-up, document generation and review, tracking of samples enrollment of study participants, a