Top 931 Development associate Jobs in Princeton, Nj

Associate Director, Clinical Research
Bracco —Princeton, NJ
- Full-time
- Hybrid work
- Bachelor of Science
- Senior level
- Communication skills
Associate Veterinarian
Global Veterinary Careers —Yardley, PA
- $120,000 - $180,000 a year
- Full-time
- Surgery
- In-person
- Entry level
- Continuing education credits
- Relocation assistance
Quick Apply
11d
Associate Attorney - Insurance Coverage & Defense
Orion Placement —Bensalem, PA
- $155,000 - $195,000 a year
- Full-time
- Writing skills
- Mid-level
- Analysis skills
- Free parking
- Health savings account
Quick Apply
Associate Attorney - Insurance Coverage & Defense
Orion Placement —Yardley, PA
- $155,000 - $195,000 a year
- Full-time
- Writing skills
- Mid-level
- Analysis skills
- Free parking
- Health savings account
Quick Apply
Teacher-Mid Level
Early Learning Children's Academy —Doylestown, PA
- $21 - $26 an hour
- Full-time
- Background check
- Classroom
- CPR Certification
- Health insurance
- Dental insurance
Quick Apply
Associate Veterinarian
Global Veterinary Careers —Woodbridge, NJ
- $120,000 - $180,000 a year
- Full-time
- Mid-level
- Surgery
- In-person
- Continuing education credits
- Relocation assistance
Quick Apply
11d
Associate Attorney – Consumer Bankruptcy & Debt Resolution
Orion Placement —Edison, NJ
- $75,000 - $120,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Dental insurance
- Paid time off
Quick Apply
Associate Director, Companion Diagnostics Leader
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $166,720 - $250,080 a year
- Bachelor of Science
- Analysis skills
- Bachelor's degree
Associate Director, Statistical Programming - R Implementation
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $171,120 - $256,680 a year
- 7 years
- Computer Science
- Master's degree
14d
Teacher-Mid Level
Early Learning Children's Academy —Bensalem, PA
- $20 - $27 an hour
- Full-time
- Background check
- Classroom
- CPR Certification
- Health insurance
- Dental insurance
Quick Apply
Associate Director, Regulatory Affairs Advertising and Promotion
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $166,720 - $250,080 a year
- Office
- Bachelor's degree
- Continuous improvement
NJ Civil Defense Litigation Associate (3+ Years)
Gfeller Laurie LLP —Princeton, NJ
- From $140,000 a year
- Full-time
- Hybrid work
- Background check
- Writing skills
- Mid-level
- Health savings account
- Paid holidays
Quick Apply
5d
Career Service Associate
Pennco Tech —Bristol, PA
- $37,400 - $42,000 a year
- Full-time
- University
- In-person
- Associate's degree
- Health insurance
- Dental insurance
Quick Apply
6d
Associate Director, Clinical Science
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $162,400 - $243,600 a year
- Office
- Master's degree
- Bachelor's degree
Associate Director, Biostatistics (Late Stage Oncology)
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $175,440 - $263,160 a year
- 5 years
- Office
- Master's degree
14d
Yard Associate
PERI —Bridgewater, NJ
- $19.50 an hour
- 8 hour shift
- Ability to walk for extended periods
- Basic math
- Maintenance
- Paid holidays
- Health insurance
Associate Director, Clinical Data Management
Genmab —Princeton, NJ
- $157,360 - $236,040 a year
- Online Application
- Analysis skills
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave
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
Overnight Senior Mental Health Associate
The Center for Great Expectations —Somerset, NJ
- $22 an hour
- Overnight shift
- Inventory management
- Mid-level
- Office
- Paid holidays
- Health insurance
Quick Apply
Associate Director - External Data Acquisition Lead (EDAL)
Genmab —Plainsboro, NJ
- $157,360 - $236,040 a year
- Online Application
- Master's degree
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave

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development associate jobs near princeton, nj

Associate Director, Clinical Research

Bracco -
Princeton, NJ

Apply Now

Job Details

Full-time

Qualifications

Project team coordination
Data integrity assurance
Biology
Data quality checks
Medical writing
Biochemistry
Informed consent
Team supervision
Document control experience within pharmaceutical industry
Adverse event reporting
Clinical incident reports
Bachelor of Science
Filing
Ordering medications
Research project design
Patient safety
Bachelor's degree in biology
Invoice payment processing
ICH guidelines
Vendor compliance management
Research safety & compliance
Clinical training
Scientific protocols
Team training
Data quality monitoring
Invoice reconciliation
Managing clinical research teams
Vendor communication
Pharmacy
Leading team collaboration initiatives

Full Job Description

Bracco Diagnostics Inc. is a subsidiary of Bracco Imaging which is part of the overall Bracco Group. The Company specializes in the clinical development, marketing and sales of diagnostic contrast imaging agents. Bracco Diagnostics Inc. primarily markets its products to hospitals throughout the United States. Bracco Diagnostics Inc. is committed to the discovery, development, manufacturing and marketing of imaging agents and solutions aimed at providing a better use and management in terms of diagnostic efficacy, patient safety and cost effectiveness.

The Associate Director/ Director, Clinical Research leads and manages end-to-end clinical research activities for assigned programs and studies, ensuring compliance with regulatory standards (ICH/GCP) and study protocols. Oversees study design, site selection, vendor and CRO management, and clinical operations, while coordinating investigators, monitoring study progress, and maintaining data quality and documentation. Ensures timely execution, budget adherence, regulatory compliance, and effective communication across internal teams, study sites, and external partners.

The Associate Director/ Director, Clinical Research is person is responsible for leading clinical research activities for a specific program or programs as well as managing all activities associated with performing one or more clinical studies. This person has the responsibility to guide and supervise clinical research activities performed by external vendors (CROs), consultant monitors (when applicable) and clinical study assistants working on assigned projects.

Main Responsibilities, Activities, Duties, and Tasks

Writing and finalizing protocols for the conduct of interventional clinical studies and noninterventional studies as well as studies designed for the retrospective collection of data
Identifying, selecting, and qualifying sites to conduct clinical studies
Reviewing informed consent forms and other Study Master File (TMF) documents, ensuring that all regulatory requirements are met
Performing site visits including monitoring activities as needed/assigned, ensuring the clinical study is being performed according to ICH/GCP guidelines and meeting the protocol requirements
Planning, coordinating, and facilitating investigator meetings
Communicating with study centers, addressing issues, and disseminating study study information
Training investigators, monitors and site personnel to ensure appropriate collection and reporting of non-serious and serious adverse events, as well as special situations, and any urgent safety measures taken by the site during the study
Assisting with data flow and query resolution
Requesting and managing clinical supplies, including coordinating the shipment of the clinical supplies to study sites, over-seeing drug accountability and the return of clinical supplies to Bracco
Managing vendors and consultants (e.g., central ECG and central lab services)
Ensuring that all project information is up to date in the Clinical Study Management System (CTMS) (e.g., monitoring visits; enrollment)
Ensuring the current version of project documentation is filed in Expresso
Tracking enrollment for each site; proactively addressing issues, insuring protocol compliance
Maintaining the TMF
Initiating payments to investigators
Overseeing payments to vendors: reviewing invoices including documentation supporting pass through costs
Overseeing the tracking of receipt of original CRFs in house at Bracco
Submitting SUSARs to IRBs/ECs and Investigators as needed
Ensuring that projects keep within their approved budget
Communicating critical study-related or personnel issues to the Head of Worldwide Clinical Research in a timely manner to facilitate immediate action
Reviewing, revising, and facilitating the training / approval process for clinical related SOPs

Supervisory Responsibilities

Education

B.S./B.A. degree preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)

Professional Experience, Knowledge & Technical Skills

10+ years Clinical Research/Management experience with demonstrated experience in multinational and/or multi-site clinical studies. Knowledge of GCPs, CFR, ICH and EU guidelines
Strong organizational, communication and teamwork skills. Ability to manage several projects simultaneously. Experience in diagnostic imaging field is desired.
Ability to manage multiple projects/programs simultaneously
Ability to manage investigators, consultants, vendors
Excellent written and verbal communication skills with particular attention to communicating study information
Taking personal responsibility to achieve results/objectives and makes every effort to achieve the expected outcome of any task
Ability to work independently, with minimum supervision
Ability to work in a team
Ability to deal with competing priorities, meet aggressive timelines within the assigned scope of the project

Core Relationships

Medical Planning and Management
Medical Affairs and Scientific Information
Data Management
Biostatistics
Regulatory Affairs &Medical Writing
Corporate Drug Safety
Management Office
Corporate Quality Management
Clinical Research Quality Systems
Global Legal Affairs

Work Environment

The work environment characteristics described here are representative of those an employee

encounters while performing the essential functions of this job. Reasonable accommodations may

be made to enable individuals with disabilities to perform the essential functions. The employee must be able to communicate via telephone, written correspondence, or spoken word to perform the essential duties of the position .

Bracco Diagnostics Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, or any other protected status.

Apply Now

Refine Your Search

development associate jobs in princeton, nj

Associate Director, Clinical Research

Associate Veterinarian

Associate Attorney - Insurance Coverage & Defense

Associate Attorney - Insurance Coverage & Defense

Teacher-Mid Level

Associate Veterinarian

Associate Attorney – Consumer Bankruptcy & Debt Resolution

Associate Director, Companion Diagnostics Leader

Associate Director, Statistical Programming - R Implementation

Teacher-Mid Level

Associate Director, Regulatory Affairs Advertising and Promotion

NJ Civil Defense Litigation Associate (3+ Years)

Career Service Associate

Associate Director, Clinical Science

Associate Director, Biostatistics (Late Stage Oncology)

Yard Associate

Associate Director, Clinical Data Management

Associate Director, Clinical Data Management

Overnight Senior Mental Health Associate

Associate Director - External Data Acquisition Lead (EDAL)

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