- Parexel (Jackson, MS)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable… more
- Parexel (Jackson, MS)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures...in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of essential… more
- Parexel (Jackson, MS)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for… more
- Parexel (Jackson, MS)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures...in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of essential… more
- Parexel (Jackson, MS)
- …ensure site readiness for First Subject First Visit (FSFV) + Partners with Clinical Research Associate (CRA) to ensure site monitoring readiness in anticipation ... ICH-GCPs, and other applicable requirements **Skills:** + Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements + Must… more
- Parexel (Jackson, MS)
- …+ RWD/RWE expertise, commercial experience, and familiarity with late-phase clinical research. + Understanding of RWD platforms, project management systems, ... and GCP environments. **Education:** Bachelor's degree in a science or clinical -related field; Prince II or AMPM certification preferred. **Why Join Us?** + **Career… more
- Parexel (Jackson, MS)
- …we are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director, you will work closely with...the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical… more
- GRAIL (Jackson, MS)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... + **Experience** + Minimum of 10 years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device, or… more
- Parexel (Jackson, MS)
- …Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as primary client contact for ... and support of junior medical writing staff. **Key Accountabilities** : **Author Clinical Documents** + Gather, review, analyze, and evaluate pertinent resources to… more
- Fujifilm (Jackson, MS)
- **Position Overview** The Associate Clinical Specialist independently provides customer support of Fujifilm's ES equipment in the Endoscopy department and/or ... catalog for assigned customers. It serves as the primary clinical resource for the Company and its sales team...and prevent future handling damages. + Serve as a clinical liaison by developing and delivering comprehensive weekly and… more
- Sumitomo Pharma (Jackson, MS)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . The ... director is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators and key… more
- Merck (Jackson, MS)
- …fully dedicated to training and education activities supporting the monitoring roles in clinical operations eg Clinical Research Associate (CRAs), ... highly motivated individuals to join our team for a Clinical Operations Educator position. As Clinical Operations...Clinical Research Managers (CRMs), in the Global Clinical Trial Operations (GCTO) Regions in alignment with strategic… more
- Medtronic (Jackson, MS)
- …resume._ + High School Diploma or GED AND a minimum of 8 years of patient care/ clinical experience; or + Associate 's Degree AND a minimum of 6 years of patient ... valid driver's license is essential for this role. At Medtronic, the Senior Clinical Specialist supports the Pelvic Health groups in the areas of surgical coverage,… more
- CenterWell (Jackson, MS)
- …part of our caring community and help us put health first** The Associate Director, Product Management Conceives of, develops, delivers, and manages products for ... customer use. The Associate Director, Product Management requires a solid understanding of...dynamic team of product management professionals dedicated to advancing clinical operations and technology solutions. Drive the strategic roadmap… more
- Sumitomo Pharma (Jackson, MS)
- …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable ... to ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements.… more
- Otsuka America Pharmaceutical Inc. (Jackson, MS)
- …needs and nutraceutical products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and ... responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a… more
- Sumitomo Pharma (Jackson, MS)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical … more
- Otsuka America Pharmaceutical Inc. (Jackson, MS)
- **Job Summary** The Associate Director, Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's… more
- CenterWell (Jackson, MS)
- …of members who need it the most. We're a fast-growing organization changing how clinical care is delivered - using innovation, data, and technology to keep patients ... to challenge the status quo in healthcare. About the Role We're seeking a Clinical Operations Lead for CenterWell Medical Group who brings energy, creativity, and a… more
- Otsuka America Pharmaceutical Inc. (Jackson, MS)
- The Associate Director, Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic area ... and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory, Commercial). **Content Execution Direction** + Provide… more
