Clinical documentation specialist jobs in Plainfield, NJ

Primary Talent Partners has a 14 month contract opening for a Documentation Specialist to join a.. Responsibilities. Supports the operational aspects of procedural documentation management and advises on..

Innova Solutions is immediately hiring for a Documentation Specialist. III. As a Documentation.. 2. months Location. Rahway, New Jersey 07065 As a Documentation Specialist. III, your responsibilities..

Title. Documentation Specialist. III Location. Rahway NJ OR Gwynedd, PA (3 days onsite required.. 2. Months Pay rate. 45.50 hr Supports the operational aspects of procedural documentation management..

Documentation Specialist. III (Senior) Gwynedd, PA or Rahway, NJ. 3 days onsite required 2 Months.. 5.49 hr Supports the operational aspects of procedural documentation management and advises on..

Supports the operational aspects of procedural documentation management and advises on documentation.. The role is responsible for supporting Global Regulatory Affairs & Clinical Safety Document Owners and..

Position. Clinical Documentation Specialist. Department. Regulatory Affairs & Pharmacovigilance Location.. months Additional. 3 days onsite required. Job Description. The Documentation Specialist. III (Senior..

Our client, one of the largest pharmaceutical companies in USA is looking for a Documentation Specialist.. Job Title. Documentation Specialist. III Duration. 2 Month Contract Location. HYBRID, 3 days onsite..

Responsibilities. Supports the operational aspects of procedural documentation management and advises on documentation strategy for Client's Global Regulatory Affairs & Clinical Safety (GRACS..

Title. Documentation Specialist Location. Rahway, NJ. Upper Gwynedd, PA Duration. 12 months. Description.. Description. Supports the operational aspects of procedural documentation management and advises on..

Supports the operational aspects of procedural documentation management and advises on documentation.. The role is responsible for supporting Global Regulatory Affairs & Clinical Safety Document Owners and..

Software Guidance & Assistance, Inc., (SGA), is searching for a Sr. Documentation Specialist for a Contractassignment with one of our premier Pharmaceutical Services clients in Madison, NJ..

317 Job Title. Global Regulatory Affairs Documentation Specialist Location. Rahway, NJ Duration.. Develop and manage integrated project plan. Lead & or complete documentation impact assessments to..

The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study.. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS..

Knowledge of experience with CTMS EDC TMF. Experience with Good Clinical Practice (GCP). Oversees.. Conducts registered and nonregistered clinical studies of products that have been determined to satisfy..

The Clinical Donation Specialist is responsible for facilitating the organ and tissue donor process.. Facilitates the organ recovery process in the Operating Room including reviewing documentation according..

Summary This position is part of Chemistry, Manufacturing, and Controls (CMC) Documentation and Specifications (CDS) group. The selected candidate will provide support creating workflows and..

Job Description The Technical Writer and Document Specialist (TW DS) will sit within the Cell Therapy.. This individual will be responsible for delivering CMC documentation (Dossier and supporting documents..

Job Description. The Technical Writer and Document Specialist (TW DS) will sit within the Cell Therapy.. This individual will be responsible for delivering CMC documentation (Dossier and supporting documents..

Responsibilities A day in the life of a Clinical Risk and Loss Prevention Specialist at Hackensack.. Collaborate with Executive, Regional, Local, Nursing and Clinical Leadership to create a sustainable..