- Parexel (Trenton, NJ)
- …in clinical development operations or clinical trial outsourcing \#LI-LO1 \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants ... will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. more
- Parexel (Trenton, NJ)
- …Activation. Serves as the primary contact for creation and management of the Investigator and Institution Global Directory. Will play a leading role in ensuring the ... assembly and distribution of Site Administrative Binders to investigator sites at the time of site initiation/activation. **JOB DUTIES:** ** Investigator… more
- Parexel (Trenton, NJ)
- …the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance ... The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg… more
- Parexel (Trenton, NJ)
- …in the delivery of monitoring + Supports the CRA to develop positive Investigator relationships throughout the life of the study and escalate any training or ... new processes and systems + Identifies and builds effective relationships with investigator site staff and other stakeholders + Effective verbal and written… more
- Parexel (Trenton, NJ)
- …+ Experience as a Physician in Industry or as a clinical trial investigator is required + Previous CRO experience is strongly preferred + Medically qualified ... to travel 15% domestically or internationally is required \#LI-LB1 \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will… more
- Parexel (Trenton, NJ)
- …members of writing staff, prepares clinical study reports (CSRs), protocols, investigator brochures (IBs), submission data summaries, and other regulatory documents ... Bachelor's degree or equivalent (Life Science preferred) \#LI-LG4 \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants… more
- Parexel (Trenton, NJ)
- …with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA indication and ... preferred -Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is… more
- Parexel (Trenton, NJ)
- …+ Collaborates within cross functional study teams + Presents at investigator meetings and creates training materials (lab manual, sample collection procedures ... Science degree or equivalent + Biology or equivalent major preferred \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will… more
- Parexel (Trenton, NJ)
- …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature reviews, ... in a wide range of disciplines Education: - BA/BS or higher \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive… more
- Parexel (Trenton, NJ)
- …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature reviews, ... documents **Education:** + BA/BS, Advanced degree preferred \#LI-LO1 \#LI-REMOTE EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants… more
- City of New York (New York, NY)
- …DOF's Equal Employment Opportunity Office is seeking a qualified individual to serve as an EEO Investigator . The individual will report directly to the EEO ... compliance while providing exceptional customer service. The Equal Employment Opportunity ( EEO ) Office ensures compliance with federal, state, and city EEO… more
- City of New York (New York, NY)
- …perform the essential functions of their job. OEEO is currently seeking to hire an EEO Attorney Investigator that will report to the EEO Supervising Attorney ... interested in diversity, equity, and inclusion in the workplace. The EEO Attorney Investigator will be responsible for investigating EEO violations in… more
- Parexel (Trenton, NJ)
- …Activation. Serves as the primary contact for creation and management of the Investigator and Institution Global Directory. Will play a leading role in ensuring the ... assembly and distribution of Site Administrative Binders to investigator sites at the time of site initiation/activation. **JOB DUTIES:** ** Investigator… more
- City of New York (New York, NY)
- Job Description APPLICANTS MUST BE PERMANENT IN THE ASSOCIATE FRAUD INVESTIGATOR CIVIL SERVICE TITLE. The DSS Accountability Office (DSS-AO) is responsible for ... levels. C&C is recruiting for (1) one Associate Fraud Investigator II to function as a Group Supervisor, who...time and leave. Evaluate job performance and compliance with EEO & other agency mandates. Meet with staff regularly… more
- City of New York (New York, NY)
- …school graduate interested in starting a career in equal employment opportunity ( EEO ) investigation and program initiatives. The qualified candidate will join the ... EEO and Fair Housing (FH) Investigations Unit as an Attorney Interne Investigator reporting to a Deputy Director and dotted line report to the Vice President & … more
- Bristol Myers Squibb (Princeton, NJ)
- …prepares study protocols, amendments, specific sections of study manuals and Investigator meeting materials, and other documents as needed with appropriate guidance ... the preparation/review of INDs, regulatory documents, IND annual report/DSURs, Investigator Brochures, and NDAs/MAAs. + Supports priorities within functional area.… more
- Sumitomo Pharma (Trenton, NJ)
- …CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contribute to content as needed… more
- Sumitomo Pharma (Trenton, NJ)
- …CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contribute to content as needed… more
- Sumitomo Pharma (Trenton, NJ)
- …writing of clinical study reports + Contributes to the preparation of Investigator Brochures, annual reports, data collection systems and final reports in compliance ... globally + Contributes to the development of presentation materials for investigator meetings, health authority meetings, scientific advisory board meetings, and… more
- Pfizer (New York, NY)
- …related documents, including but not limited to clinical development plan, investigator brochure, statistical analysis plan and regulatory documents. + Conducts data ... WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS** Travel may be required for investigator meetings US/EX; US for presenting protocol for research sites. Relocation… more
