Top 21 Principal statistical Jobs in Bridgewater, Nj

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
FSP Principal Statistical Programmer (Remote)
Everest Clinical Research —Bridgewater, NJ
- $112,000 - $175,000 a year
- Remote
- Computer Science
- Doctor of Philosophy
- Mentoring
- AD&D insurance
- Disability insurance
Quick Apply
Principal Statistical Programmer (Remote)
Everest Clinical Research —Bridgewater, NJ
- $112,000 - $175,000 a year
- Remote
- Computer Science
- Doctor of Philosophy
- Mentoring
- AD&D insurance
- Disability insurance
Quick Apply
Principal Biostatistician (Remote)
Everest Clinical Research —Bridgewater, NJ
- $150,000 - $200,000 a year
- Remote
- 7 years
- Master's degree
- Continuous improvement
- AD&D insurance
- Disability insurance
Quick Apply
11d
Principal Statistical Programmer
Regeneron —Warren, NJ
- $109,900 - $179,300 a year
- 3 years
- Master's degree
- Quality control
- Health insurance
- Dental insurance
Sr Principal / Principal Scientist Personal Care Formulation & Implementation (174499)
Colgate-Palmolive —Piscataway, NJ
- $124,000 - $174,000 a year
- Hybrid work
- Master's degree
- Databases
- Bachelor's degree
- Profit sharing
- Paid parental leave
5d
Senior Principal Statistical Programmer
Katalyst Healthcares & Life Sciences —Newark, NJ
- Contract
- 6 years
- Doctor of Philosophy
- Organizational skills
Quick Apply
Principal Data Manager I
Everest Clinical Research —Bridgewater, NJ
- $130,000 - $165,000 a year
- Remote
- Bachelor of Science
- Bachelor's degree
- Training & development
- AD&D insurance
- Disability insurance
Quick Apply
Associate Principal Scientist, Biologics Analytical R&D
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- Bachelor of Science
- 3 years
- Analysis skills
- Paid holidays
- Health insurance
6d
Associate Principal Scientist – Bioassay, Cell Based Sciences, AR&D
Merck —Rahway, NJ
- $142,400 - $224,100 a year
- Full-time
- Bachelor of Science
- Analysis skills
- Bachelor's degree
- Paid holidays
- Health insurance
10d
Principal Scientist, Technical Project Leader
Experic LLC —Cranbury, NJ
- $135,000 - $175,000 a year
- 3 years
- Math
- Doctor of Philosophy
Quick Apply
Principal Clerk, Family Health Services, Mother/Baby - F Green (8am-5=4pm)
University Hospital, Newark NJ —Newark, NJ
- Full-time
- Word processing
- English
- Mid-level
Quick Apply
Principal Scientist – Solubility Enhancement Technologies
Ardena —Somerset, NJ
- Hybrid work
- Bachelor of Science
- 3 years
- Bachelor's degree
Principal Scientist, Data Science and AI - Princeton, NJ
dsm-firmenich —Princeton, NJ
- Online Application
- English
- Doctor of Philosophy
- Mentoring
Associate Principal Analyst, Advertising Regulation
Financial Industry Regulatory Authority, Inc. —Woodbridge, NJ
- $83,900 - $180,400 a year
- Extended hours
- Hybrid work
- Microsoft Word
- Management
- 5 years
- Paid jury duty
- Commuter assistance
Quick Apply
Principal Data Scientist, Digital Innovation - Predictive Formulations
Ingredion Incorporated —Bridgewater, NJ
- $123,500 - $164,700 a year
- Full-time
- Analysis skills
- Mentoring
- Senior level
- Health insurance
- Dental insurance
Quick Apply

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principal statistical jobs near bridgewater, nj

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

principal statistical jobs in bridgewater, nj

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

FSP Principal Statistical Programmer (Remote)

Principal Statistical Programmer (Remote)

Principal Biostatistician (Remote)

Principal Statistical Programmer

Sr Principal / Principal Scientist Personal Care Formulation & Implementation (174499)

Senior Principal Statistical Programmer

Principal Data Manager I

Associate Principal Scientist, Biologics Analytical R&D

Associate Principal Scientist – Bioassay, Cell Based Sciences, AR&D

Principal Scientist, Technical Project Leader

Principal Clerk, Family Health Services, Mother/Baby - F Green (8am-5=4pm)

Principal Scientist – Solubility Enhancement Technologies

Principal Scientist, Data Science and AI - Princeton, NJ

Associate Principal Analyst, Advertising Regulation

Principal Data Scientist, Digital Innovation - Predictive Formulations

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