Top 49 Clinical trial manager Jobs in Gladstone, Nj

Clinical Trial Manager/Senior Clinical Trial Manager
Precision for Medicine —Gladstone, NJ
- $110,700 - $200,900 a year
- Online Application
- Remote
- 7 years
- Microsoft Excel
- Microsoft Outlook
Quick Apply
10d
Clinical Trial Manager/Senior Clinical Trial Manager
Precision Medicine Group —Gladstone, NJ
- $110,700 - $200,900 a year
- Online Application
- Remote
- 7 years
- Microsoft Excel
- Microsoft Outlook
10d
Clinical Trial Liaison Manager
Recordati —Bridgewater, NJ
- $109,800 - $164,700 a year
- Weekends as needed
- Hybrid work
- 5 years
- English
- Mid-level
- AD&D insurance
- Paid holidays
Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
Junior / Lower Mid-Level - Clinical Trial Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Microsoft Outlook
- English
- Mid-level
Quick Apply
4d
Clinical Program Manager
IQVIA —Parsippany-Troy Hills, NJ
- $93,100 - $285,500 a year
- Full-time
- Remote
- Bachelor's degree
- Conflict management
- Senior level
- Work from home
Title Clinical Trial Liaison Manager
Recordati —Bridgewater, NJ
- $109,800 - $164,700 a year
- Weekends as needed
- Hybrid work
- 5 years
- English
- Mid-level
- AD&D insurance
- Paid holidays
Clinical Program Manager
Kite Pharma —Parsippany-Troy Hills, NJ
- $165,495 - $235,620 a year
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Dental insurance
Contracts Manager, Clinical Supply Services
Catalent —Bridgewater, NJ
- $122,000 - $160,000 a year
- Email
- Writing skills
- Mid-level
- Office
- Paid holidays
- Health insurance
6d
CLINICAL DATA MANAGER
Zenith LifeScience —South Plainfield, NJ
- $100,000 - $120,000 a year
- Full-time
- Bachelor of Science
- Math
- Bachelor's degree
Senior Clinical Drug Supply Manager
Amneal Pharmaceuticals —Bridgewater, NJ
- $170,000 - $190,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
- Health insurance
- 401(k) matching
4d
Senior Project Manager - Oncology
Precision Medicine Group —Gladstone, NJ
- $147,300 - $220,900 a year
- Online Application
- Remote
- Microsoft Excel
- Microsoft Outlook
- Master's degree
Project Manager, eCOA Implementation
IQVIA —Wayne, NJ
- $88,100 - $220,200 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Mentoring
- Work from home
12d
Senior Project Manager - Oncology
Precision for Medicine —Gladstone, NJ
- $147,300 - $220,900 a year
- Online Application
- Remote
- Microsoft Excel
- Microsoft Outlook
- Master's degree
Quick Apply
Senior Manager, Clinical Data Systems
AbbVie —Florham Park, NJ
- $124,500 - $236,500 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- SQL
- Paid holidays
- Health insurance
Manager, Clinical Study Lead
Regeneron —Warren, NJ
- $128,600 - $210,000 a year
- Microsoft Word
- Microsoft Excel
- 6 years
- Health insurance
- Dental insurance
Clinical Study Associate Manager
Regeneron —Warren, NJ
- $109,900 - $179,300 a year
- Bachelor's degree
- Team management
- Travel
- Health insurance
- Dental insurance
Senior Manager, GCP QA
Shionogi Inc. —Florham Park, NJ
- $135,000 - $165,000 a year
- Email
- Hybrid work
- Management
- 5 years
- Bachelor of Science
Sr.Clinical Data Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Hybrid work
- Nursing
- Bachelor's degree
- Senior level
Quick Apply
Senior Manager, External Research Program (ERP)
Kite Pharma —Parsippany-Troy Hills, NJ
- $153,935 - $199,210 a year
- Full-time
- Microsoft Word
- Master's degree
- High school diploma or GED
- Health insurance
- Dental insurance

I want to receive the latest job alert for clinical trial manager in gladstone, nj

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical trial manager jobs near gladstone, nj

Clinical Trial Manager/Senior Clinical Trial Manager

Precision for Medicine -
Gladstone, NJ

Quick Apply

Job Details

$110,700 - $200,900 a year
10 days ago

Qualifications

Microsoft Excel
Microsoft Outlook
Pharmaceutical research experience
Delegation

Full Job Description

Position Summary:

Serves as the clinical trial lead responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work and ensures that clinical studies are conducted in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP and all applicable regulatory requirements.

Essential functions of the job include but are not limited to:

Primary clinical point of contact with the client
Collaborate with PM on monthly invoicing and variance management of clinical budget
Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials)
Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings
Generate potential site list from key stakeholders and drive site feasibility process
Identify potential risks to the enrollment targets based on feasibility analysis and site's contracted commitment
Develop and finalize the country recruitment/retention strategy
Develop timely and effective communication and good working relationships with investigators and study team to ensure effective and timely feasibility, site start up, enrollment, maintenance and close out procedures
Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs
Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate
Support in planning and conducting investigator meetings
Review and/or approve of IP release packages
Oversee, support and track all submissions and approvals to Competent Authorities and IRB/Ethics Committees in conjunction with regulatory departments as applicable
Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables
Generate and utilizes metric reporting (e.g., CTMS, DM Query Trends, Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to PM and CRAs as appropriate
Responsible for eTMF implementation and management
Collaborate with PM, CRAs and QA to develop any Corrective and Preventative Action Plan (CAPA) and is accountable for implementation and timely closure
Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits
Work closely with PM for project-specific resourcing issues
Escalate pertinent CRA performance and site compliance issues when necessary
Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines
Manage processes for investigational product (IP) including drug accountability and reconciliation
When a cross-functional PM is not assigned to a given program, the CTM will assume project management responsibility as needed
Support business development and marketing activities as appropriate
May negotiate site budget and investigator contract with support from the legal department and/or site contracts group
May review site visit reports and ensures monitoring (i.e. scheduling and scope) is executed per monitoring plan
May be responsible for management of clinical vendors (e.g. labs, IP, patient diary, home health care) in conjunction with PM
May perform clinical data review of patient profiles, data listings and summary tables, including query generation
May have line management responsibilities
Performs other duties as assigned by management

Qualifications:

Minimum Required:

Bachelor's degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred
Minimum of 7 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience

Preferred:

Advanced degree

Other Required:

Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint)
Excellent communication and interpersonal skills to effectively interface with others in a team setting
Excellent organizational skills, attention to detail, and a customer service demeanor
Ability to travel domestically and internationally including overnight stays

Competencies:

Demonstrates mastery knowledge of ICH-GCP, relevant Precision SOPs, and regulatory guidance, as well as the ability to implement
Working knowledge of clinical management techniques and tools
Direct work experience in a cross-functional environment
Proven experience in functional management including proven experience in delegating while fostering cohesive team dynamics
Proven experience in planning, risk management and change management
High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective
Ability to lead and inspire excellence within a team
Ability to create an environment where employees have a sense of ownership that will lead to increases in productivity and efficiency
Results oriented, accountable, motivated and flexible
Excellent time management, negotiation, critical thinking, decision making, analytical and interpersonal skills
Excellent presentation, verbal and written communications skills
In depth proven experience in pharmaceutical and/or device research required
Demonstrated successful independent negotiation and conflict management strategies

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Quick Apply

Refine Your Search

clinical trial manager jobs in gladstone, nj

Clinical Trial Manager/Senior Clinical Trial Manager

Clinical Trial Manager/Senior Clinical Trial Manager

Clinical Trial Liaison Manager

Senior Clinical Trial Manager

Junior / Lower Mid-Level - Clinical Trial Manager

Clinical Program Manager

Title Clinical Trial Liaison Manager

Clinical Program Manager

Contracts Manager, Clinical Supply Services

CLINICAL DATA MANAGER

Senior Clinical Drug Supply Manager

Senior Project Manager - Oncology

Project Manager, eCOA Implementation

Senior Project Manager - Oncology

Senior Manager, Clinical Data Systems

Manager, Clinical Study Lead

Clinical Study Associate Manager

Senior Manager, GCP QA

Sr.Clinical Data Manager

Senior Manager, External Research Program (ERP)

I want to receive the latest job alert for clinical trial manager in gladstone, nj

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected