- Daiichi Sankyo, Inc. (Bernards, NJ)
- …labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads ... the development and maintenance of the CCDS , US and EU labeling, and manages the review...new and updated Core Data Sheets, EU and US Documentation : As the project lead, Independently or through direction… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data ... Sheets ( CCDS ) for assigned products. This position drives/leads the maintenance...of updated Core Data Sheets, and EU and US Documentation : Independently manages, prepares and implements regulatory documents (eg,… more
- Northwell Health (Lake Success, NY)
- **Req Number** 134398 Job Description Directs the activities of the Clinical Documentation Improvement (CDI) department. Facilitates modifications to clinical ... case management, and medical records coding staff. Job Responsibility + Leads a Clinical Documentation group by communicating with and developing staff members,… more
- Catholic Health Services (Rockville Centre, NY)
- …Responsible for improving the overall quality and completeness of clinical documentation through self-direction and self-management. Facilitates clarification ... to the clinical documentation through extensive interaction with physicians,...Expert knowledge of CDI chart review and query policy CCDS certified Proficient in quality metrics as it relates… more
- Takeda Pharmaceuticals (Columbus, OH)
- …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... and updates to or creation of a new TLP, CCDS , USPI and EU SmPC, with limited supervision and...all relevant functional areas with appropriate annotations and supporting documentation with appropriate supervision and guidance. + With adequate… more
- AdventHealth (Altamonte Springs, FL)
- …Location** : Remote **The role you'll contribute:** Under general supervision of the Director of Clinical Documentation Integrity and in some situations ... ECFMG Certification and examination at the time of graduation . CCDS (Certified Clinical Documentation Specialist) certification, or/and CDIP (Certified … more
- Hackensack Meridian Health (Neptune, NJ)
- …and/or strong Medical/Surgical experience. **Licenses and Certifications Required:** + Certified Clinical Documentation Specialist ( CCDS ) or certification ... two (2) years of eligibility. **Licenses and Certifications Preferred:** + Certified Clinical Documentation Specialist ( CCDS ) or certification within two… more
- AdventHealth (Altamonte Springs, FL)
- …(CDI) Implementation Specialist and Educator who, under the direction of the corporate Director of Clinical Documentation Integrity and in some cases ... for ECFMG Certification and examination at the time of graduation. . Certified Clinical Documentation Specialist, CCDS and/or Certified Documentation … more
- AdventHealth (Glendale Heights, IL)
- …training/education as needed **The role you'll contribute:** Under general supervision of the Director of Clinical Documentation Integrity and in some ... at the time of graduation. **LICENSURE, CERTIFICATION OR REGISTRATION PREFERRED** * CCDS (Certified Clinical Documentation Specialist) certification * CDIP… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data ... Sheets ( CCDS ) for assigned products. This position drives/leads the maintenance...of updated Core Data Sheets, and EU and US Documentation : Independently manages, prepares and implements regulatory documents (eg,… more
- BeiGene (Emeryville, CA)
- The Executive Medical Director serves as the Lead Product Safety Physician for multiple or large complex strategically important developmental programs (often ... support of Safety Physicians and Safety Scientists identifies and manages the documentation and communication of safety concerns and together with teams engaged in… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , RA Labeling Product Leader (1 of 2) - 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate ... Director , RA Labeling Product Leader (1 of 2) in...maintenance of primary labeling (the Company Core Data Sheet ( CCDS ), United States Package Insert (USPI) and associated patient… more
- AbbVie (Florham Park, NJ)
- …regulatory, clinical and safety. Manages labeling history and negotiation documentation for assigned products. Provides labeling strategy and direction to teams ... on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and… more
- Granville Health System (Oxford, NC)
- …is responsible for improving the overall quality and completeness of our clinical documentation . The CDI Specialist is responsible for interacting with ... and other audit programs, recognizing and disseminating to physicians the importance of clinical documentation for both the physician and the hospital.# #Reviews… more
- HCA Healthcare (Nashville, TN)
- …or Registered Health Information Technician (RHIT), or Registered Nurse, or Certified Clinical Documentation Specialist ( CCDS ), or Cert Documentation ... as we do. We want you to apply! **Job Summary and Qualifications** The Clinical Documentation Improvement Manager is responsible for the day-to-day management of… more
- Community Health Systems (Tucson, AZ)
- …Market Supervisor, Day Shift position supporting Northwest Medical Center.** The Clinical Documentation Improvement Specialist (CDIS) Supervisor provides support ... unit, intensive care). At least 2 years experience in clinical documentation improvement, ICD 10 coding and...or compact state license. Preferred: RHIT, RHIA, CDIP, CDIS, CCDS , CCS and ICD-10 certification or designation. _Northwest Medical… more
- Community Health Systems (Tucson, AZ)
- …Shift CDI Specialist Lead opportunity supporting Northwest Medical Center!** The Clinical Documentation Improvement Specialist (CDIS) Lead provides support of ... unit, intensive care). At least 2 years experience in clinical documentation improvement, ICD 10 coding and...or compact state license. Preferred: RHIT, RHIA, CDIP, CDIS, CCDS , CCS and ICD-10 certification or designation. _Northwest Healthcare… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …(edaravone) oral suspension in 2022. The company handles research, clinical development, sales, marketing, medical affairs, supply chain,and business development ... working closely with Drug Safety Global Safety Team (GST) Chair (Medical Director ). The Manager, Drug Safety will perform signal management process activities for… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Clinical Development and Medical Affairs Fellow is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical functions ... but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology, and regulatory… more