Top 358 State investigator Jobs in New Jersey

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos - Clinical and Corporate - Prod —New Jersey
- $95,000 - $210,900 a year
- Full-time
- Microsoft Word
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Casualty Field Investigator
CUSTARD INSURANCE ADJUSTERS —Cherry Hill, NJ
- $50,000 - $65,000 a year
- Full-time
- Customer service
- Mid-level
- Office
- Health savings account
- Health insurance
Quick Apply
Associate Director, Clinical Data Management
BMS —Princeton, NJ
- $170,800 - $206,968 a year
- Email
- Hybrid work
- 7 years
- Analysis skills
- Bachelor's degree
- Paid holidays
- Disability insurance
Compliance Investigator & Licensing Specialist
21 PLUS INC —Manchester, NJ
- $27 - $28 an hour
- Weekends as needed
- 18 years or older
- Experience working with individuals with developmental disabilities
- Pass drug screening
- Paid training
- Health insurance
Quick Apply
Director, Clinical Operations - AAV
Rocket Pharmaceuticals —Cranbury, NJ
- $196,000 - $294,000 a year
- Full-time
- Microsoft Outlook
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
10d
Director, Global Clinical Physician - Late Oncology
BMS —Princeton, NJ
- $275,630 - $333,998 a year
- Email
- Hybrid work
- Medicine
- 5 years
- Analysis skills
- Paid holidays
- Disability insurance
Associate Director, Biostatistics
Genmab —Princeton, NJ
- $156,880 - $235,320 a year
- Online Application
- Master's degree
- Databases
- Doctor of Philosophy
- Commuter assistance
- Paid parental leave
UIR Coordinator
DELTA COMMUNITY SUPPORTS —Raritan, NJ
- $55,000 - $60,000 a year
- Weekends as needed
- Experience working with individuals with disabilities
- Writing skills
- Basic math
Quick Apply
Loss Prevention Investigator
Inserra Supermarkets Inc. —Ramsey, NJ
- $18 - $20 an hour
- Overtime
- 18 years or older
- High school diploma or GED
- Travel
- Health insurance
- Dental insurance
Quick Apply
Loss Prevention Investigator
Inserra Supermarkets Inc. —New Milford, NJ
- $18 - $20 an hour
- Overtime
- 18 years or older
- High school diploma or GED
- Travel
- Health insurance
- Dental insurance
Quick Apply
Property Adjuster - Field Estimating - Toms River, NJ
Allstate —Toms River, NJ
- Remote
- Background check
- Mid-level
- Driver's License
- Tuition reimbursement
- Work from home
Loss Prevention Investigator
Inserra Supermarkets Inc. —Hackensack, NJ
- $18 - $20 an hour
- Overtime
- 18 years or older
- High school diploma or GED
- Travel
- Health insurance
- Dental insurance
Quick Apply
Director, Global Clinical Physician (Director)
BMS —Princeton, NJ
- $275,630 - $333,998 a year
- Email
- Hybrid work
- Medicine
- 5 years
- Analysis skills
- Paid holidays
- Disability insurance
Senior Liability Litigation Specialist
Travelers —Morristown, NJ
- $94,400 - $155,800 a year
- Customer service
- 3 years
- High school diploma or GED
- Wellness program
- Paid holidays
4d
Loss Prevention Investigator
Inserra Supermarkets Inc. —Bayonne, NJ
- $20 - $24 an hour
- Overtime
- 18 years or older
- High school diploma or GED
- Travel
- Health insurance
- Dental insurance
Quick Apply
Medical Science Director (Mid-Atlantic Region)
System One —Parsippany-Troy Hills, NJ
- $200,000 - $240,000 a year
- Full-time
- Hospital
- Inpatient
- Clinic
- Health insurance
- Dental insurance
Quick Apply
SIU Investigator
Centene —New Jersey
- $56,200 - $101,000 a year
- Full-time
- Remote
- 5 years
- Fair chance
- Senior level
- Paid holidays
- Health insurance
Senior Investigator, Special Investigations Unit (Aetna SIU)
CVS Health —New Jersey
- $46,988 - $112,200 a year
- Full-time
- Remote
- Research
- Mid-level
- 3 years
- Health insurance
- Dental insurance
9d
AML Investigator I
Valley National Bank —Morristown, NJ
- $62,000 - $103,300 a year
- Microsoft Outlook
- Research
- Mid-level
Quick Apply
Investigator A (Claims)
NJ Transit —Newark, NJ
- Writing skills
- Mid-level
- Driver's License
- Health insurance
- Dental insurance

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Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Syneos - Clinical and Corporate - Prod -
New Jersey

Apply Now

Job Details

Full-time
$95,000 - $210,900 a year

Benefits

Employee stock purchase plan
Company car
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Paid sick time

Qualifications

Microsoft Word
Technical writing for researchers
Medical writing
Word embeddings
Schedule management
Bachelor's degree
Project management experience in healthcare
Managing projects

Full Job Description

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

Job Summary:

The Principal Medical Writer I is responsible for the development of clinical documents for submissions to regulatory authorities globally.
Provides strategic direction to cross-functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators' Brochures [IBs], Clinical Study Reports [CSRs], and marketing authorization submission documents) accurately and consistently present key data-driven clinical messages in accordance with program goals and regulatory requirements.
Writes or provides direction and leadership to other writers to ensure the timely delivery of high quality documents that are scientifically rigorous, logically organized, and have accurate data presentation and interpretation.
Oversees the medical writing activities of multiple compounds and serves as lead writer for individual summary documents.
Has a broad understanding of clinical research processes and global regulatory document standards.
Mentors less experienced writers.
Reports to a Director of Medical Writing or above.

Responsibilities:

Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and the client authoring standards, as applicable, in adherence with study/project timelines and corporate objectives.
Manage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations.
Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents.
Review other documents associated with the assigned project(s) (eg, Protocols and Statistical Analysis Plans), as appropriate.
Participate in cross-functional process improvement initiatives.
Participate in defining and writing standard operating procedures and best practices for an efficient preparation of quality documents.
Manage internal and contract medical writing resources as required to ensure timely completion of assigned projects.
Mentor more junior medical writing staff.

Minimum Requirements and Competencies:

Bachelor's degree required. Advanced degree in a relevant scientific/clinical/regulatory field preferred.
At least 5 years of medical writing experience in the biopharmaceutical/CRO industry required or comparable experience within clinical or preclinical development.
Proficiency in organizing and communicating clinical information required with minimal oversight.
Strong organizational, time management, and project management skills are required.
Strong verbal, written, and interpersonal communication skills needed to work effectively in a team environment.
Proficient understanding and knowledge of global regulatory requirements needed and knowledge of therapeutic areas in all phases of clinical development desired.
Proficient in MS Word. Experience with an electronic document management system and templates is required.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

$95,000.00 - $210,900.00

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Apply Now

Refine Your Search

state investigator jobs in new jersey

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Casualty Field Investigator

Associate Director, Clinical Data Management

Compliance Investigator & Licensing Specialist

Director, Clinical Operations - AAV

Director, Global Clinical Physician - Late Oncology

Associate Director, Biostatistics

UIR Coordinator

Loss Prevention Investigator

Loss Prevention Investigator

Property Adjuster - Field Estimating - Toms River, NJ

Loss Prevention Investigator

Director, Global Clinical Physician (Director)

Senior Liability Litigation Specialist

Loss Prevention Investigator

Medical Science Director (Mid-Atlantic Region)

SIU Investigator

Senior Investigator, Special Investigations Unit (Aetna SIU)

AML Investigator I

Investigator A (Claims)

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