A company is looking for a Commercial Contracts Attorney to provide legal support in the financial services sector....
The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety, Data Man...
A company is looking for a Virtual Physical Therapist (PT) to support middle and high school students in Massachusetts. ...
Clinical summary and overview documents in eCTD format for global regulatory submissions, including investigational medicinal product dossiers (IMPD), investigational new drug applications (IND), clinical trial applications (CTA), marketing authorization applications (MAA), and new drug applications...
A company is looking for a licensed Therapist/Counselor for remote work opportunities....
Analytical thinker capable of making informed decisions quickly and managing multiple work streams. Are you ready to apply Make sure you understand all the responsibilities and tasks associated with this role before proceeding. Develop and maintain positive relationships with client personnel, conti...
Responsibilities include evaluation of prospective sites for solar projects; analysis of existing internal or 3rd party PV designs; solar energy system design and layout with a major focus on optimizing projects for highest development financial returns; interconnection design and equipment selectio...
Its transformative cloud-based enterprise platform enables clients to take control of their pharmacy benefits with fast, flexible and customizable solutions and real time data insights to improve operational and financial performance -- and ultimately deliver better care to patients nationwide. The ...
Interested candidates should submit their resume and cover letter to Christine Mattero, Human Resources Coordinator, at jobs@shrewsburyma. You can subscribe to job posting notifications to be automatically alerted to our latest career opportunities by clicking on the NotifyMe button. We do allow app...
Cure Healthcare is seeking a CNA / Medical Assistant - CNA/MA for positions in Jamesburg, New Jersey. Required: 2 years of recent experience in CNA/MA. ...
These individuals develop collaborative relationships and work effectively with the MA/HEOR Biostatistics Lead, HEOR and Market Access functions, protocol statisticians and programmers supporting the regulatory submissions, and other Market Access & HEOR GBDS team members. The Market Access/HEOR GBD...
Authors, edits, and provides QC review of documents to support clinical trials and regulatory submissions, which may include: Clinical study protocols and protocol amendments Clinical study reports (CSR) Investigator brochures (IB) Informed consent and assent forms Lay summaries of clinical trial re...
Clinical summary and overview documents in eCTD format for global regulatory submissions, including investigational medicinal product dossiers (IMPD), investigational new drug applications (IND), clinical trial applications (CTA), marketing authorization applications (MAA), and new drug applications...
Target Locations for the Role: Maryland, Massachusetts and New Jersey Responsibilities: Support automation projects from build phase through site installation Conduct operational acceptance testing of components Conduct customer training at customer site Conduct Green Button Go instrumentation drive...
Your application will go directly to the franchisee, and all hiring decisions will be made by the management of this franchisee. Complete job documentation accurately and in a timely manner. Maintain a clean company vehicle and operate vehicle safely and legally. High School diploma/ GED preferred. ...
Maintain patient records, complete documentation as directed, and manage filing systems. Use computer software to manage office systems and maintain records. Certified Medical Assistant (CMA) from NHA, NCCT, AAMA, or AMCA. Understand the proper function and maintenance of specialized medical equipme...
OTR Routes covering all 48 states (Majority of freight is East of I-35 but we go where the freight goes. Must live in one of these states: CT, DE, MA, VT, ME, NH, NJ, RI. ...
Essential Functions Authors, edits, and provides QC review of documents to support clinical trials and regulatory submissions, which may include: Clinical study protocols and protocol amendments Clinical study reports (CSR) Investigator brochures (IB) Informed consent and assent forms Lay summaries ...
Work closely with the Market Access leadership team and leaders from Account Management, Channel Marketing, Product Marketing, and Digital teams. Manage and co-lead ad hoc, prioritized digital automation solutions for immediate process and out improvements. Impact and influence the development of co...
The Senior Medical Writer is expected to develop and maintain a network of internal relationships with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety, Data Man...
Oversee recruiting, interviewing, onboarding, and performance management of Level 3 Service Centre Team members, while identifying skills gaps and training opportunities. The ETS (Enterprise Technology Services) Level 3 Service Operations Team Leader is responsible for overseeing the daily operation...
Authors, reviews, and/or edits documents to support clinical trials and regulatory submissions, which may include: Clinical summary and overview documents in eCTD format for global regulatory submissions, including investigational medicinal product dossiers (IMPD), investigational new drug applicati...
Execute HR plans and programs to ensure most effective utilization of HR in assigned location; interpret company HR policies and procedures, laws, and regulations; may perform duties in any of the following functional areas of HR, EEO/AAP, Staffing, Compensations/Benefits, Training, Organizational D...
Essential Functions Provides strategic input into documents and plans to support clinical operations and regulatory submissions across a range of development programs and therapeutic areas: Uses professional experience to provide advanced input into study designs, analysis plans, and regulatory subm...
Our Company will never request personal information via informal chat platforms or unsecure email. Our Company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to, and does not discriminate on the basis of, race, color, religion, creed, gend...