- Highmark Health (Jefferson City, MO)
- …Coder (CPC) + Certified Outpatient Coder (COC) + Accredited Healthcare Fraud Investigator (AHFI) **SKILLS** + Must have knowledge of provider facility payment ... methodology, claims processing systems and coding and billing proficiency + Must have understanding of technical and financial aspects of the health insurance industry + Strong personal computer skills, along with the ability to use fraud/abuse data mining… more
- Sumitomo Pharma (Jefferson City, MO)
- …Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator 's Brochures (IB), Investigator communications (Dear Health Care Provider ... + Participates/contributes to other activities such as literature evaluation, investigator site training, continuing education for internal staff, inspection/audit… more
- Grifols Shared Services North America, Inc (Columbia, MO)
- …regulatory strategy + Provide input/review of clinical documents, eg protocols, investigator 's brochures, case report forms + Participate in site/ investigator ... scientific meetings and presentations + Attend and provide medical support for investigator and consultant meetings and clinical advisory boards + Develop and manage… more
- Merck (Jefferson City, MO)
- …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and retention… more
- Sumitomo Pharma (Jefferson City, MO)
- …drug/brand development. + Identify, initiate, coordinate, evaluate and monitor investigator -sponsored studies intended to support the clinical and scientific ... products. + Help develop and manage timelines of publication plans of investigator -sponsored studies. + Assist in the identification, evaluation, and engagement of… more
- Merck (Jefferson City, MO)
- …of local data generation study concepts and protocols + Reviews investigator -initiated study proposals prior to headquarters submission (ex-USA) + Manages regional ... programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company's medicines **Required** **Qualifications** **, Skills & Experience:** **_Minimum:_** + MD, PhD, PharmD or OD (MD preferred) and recognized… more
- Merck (Jefferson City, MO)
- …final approval Worldwide Marketing Applications, Clinical Study Reports, protocols, Investigator Brochures before release from our Company to external agencies ... and investigators + Represent GRA within our Company's internal committees to provide regulatory advice and approval according to the committee charters (therapeutic area Document Review Committees (DRC), Product Development Team (PDT), Early Development Team… more
- Cognizant (Jefferson City, MO)
- …Manager to drive growth and market adoption of the TriZetto Shared Investigator Platform (SIP) - a transformative SaaS collaboration solution for clinical trial ... sponsors, sites, and investigators. This role partners closely with account executives, marketing, product teams, and clients to position SIP as the go-to platform for sponsor-site engagement across clinical trial operations. **ESSENTIAL FUNCTIONS:** 1. Serve… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- …Otsuka's clinical trials program, including registrational, post-marketing and Investigator -Sponsored Trials (ISTs), health economic outcomes research, other ... specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance. + Support other areas of the organization including Safety & Pharmacovigilance for… more
- Sumitomo Pharma (Jefferson City, MO)
- …intended for regulatory submission. For example, clinical study reports (CSRs), investigator brochures (IB), new drug application (NDA) common technical document ... (CTD) non-clinical drug metabolism, bioanalytic, and clinical pharmacology chapters, and alike. + Support clinical protocols and protocol execution, including lab manual authoring based on information received from bioanalytic laboratories, pharmacokinetic… more
- Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
- …pharmacology** sections for regulatory filings, including annual reports, investigator 's brochure, IND/NDA/BLA applications and pediatrics development plans in ... compliance with relevant guidelines and standards. + Work with pharmacometricians, support **model-based drug development (MIDD)** strategies, and provide input to PK and PK/PD modeling analysis to support dose selection, efficacy and safety assessments. +… more
- Eurofins (Columbia, MO)
- …and reactions of matter. + May assist or serve as study director, principal investigator , or project leader for GLP studies. May assist in planning the conduct of ... a study. + Instrument experience a plus, in particular LC-MS/MS. The ideal candidate would possess: + Strong computer, scientific, and organizational skills + Excellent communication (oral and written) and attention to detail + Ability to work independently… more