What You'll Work On The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination ...
What You'll Work On The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination ...
What You'll Work On The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination ...
What You'll Work On The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination ...
What You'll Work On The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination ...
What You'll Work On The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination ...
Clinical Research Site Manager The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH ...
Clinical Research Site Manager The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH ...
Clinical Research Site Manager The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH ...
Clinical Research Site Manager The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH ...
Clinical Research Coordinator, Autism Research
New York, NY · On-site
$72K - $82K/yr
... Informatics Teams, the Clinical Research Coordinator will support various data activities for ... Collaborate with SFARI Clinical Research Manager, SFARI Vice President and Senior Scientific ...
Clinical Research Coordinator, Autism Research
New York, NY · On-site
$72K - $82K/yr
... Informatics Teams, the Clinical Research Coordinator will support various data activities for ... Collaborate with SFARI Clinical Research Manager, SFARI Vice President and Senior Scientific ...
Clinical Research Coordinator, Autism Research
New York, NY · On-site
$72K - $82K/yr
... Informatics Teams, the Clinical Research Coordinator will support various data activities for ... Collaborate with SFARI Clinical Research Manager, SFARI Vice President and Senior Scientific ...
Clinical Research Coordinator, Autism Research
New York, NY · On-site
$72K - $82K/yr
... Informatics Teams, the Clinical Research Coordinator will support various data activities for ... Collaborate with SFARI Clinical Research Manager, SFARI Vice President and Senior Scientific ...
Senior Manager, Clinical Operations
Bridgewater, NJ · On-site +1
$150K - $185K/yr
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... The Senior Manager is responsible for working with the Associate/ Director, Senior/ Executive ...
Senior Manager, Clinical Operations
Bridgewater, NJ · On-site +1
$150K - $185K/yr
Everest Clinical Research ("Everest") is a full-service contract research organization (CRO ... The Senior Manager is responsible for working with the Associate/ Director, Senior/ Executive ...
Clinical Research Study Manager A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations ...
Clinical Research Study Manager A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations ...
Unblinded Clinical Research Coordinator II
Jersey City, NJ · On-site
$25.25 - $33.75/hr
Unblinded Clinical Research Coordinator DM Clinical Research, the largest privately-owned clinical ... Manage inventory, ensuring that expired items are removed from the inventory prior to expiration ...
Unblinded Clinical Research Coordinator II
Jersey City, NJ · On-site
$25.25 - $33.75/hr
Unblinded Clinical Research Coordinator DM Clinical Research, the largest privately-owned clinical ... Manage inventory, ensuring that expired items are removed from the inventory prior to expiration ...
As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from ...
As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from ...
As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from ...
As the Project Manager, Clinical Research - New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from ...
Clinical Research Assistant
$24 - $29/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Assistant
$24 - $29/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Unblinded Clinical Research Coordinator II
$26.50 - $35.25/hr
Unblinded Clinical Research Coordinator II DM Clinical Research is looking for an Unblinded ... Manage inventory, ensuring that expired items are removed from the inventory prior to expiration ...
Unblinded Clinical Research Coordinator II
$26.50 - $35.25/hr
Unblinded Clinical Research Coordinator II DM Clinical Research is looking for an Unblinded ... Manage inventory, ensuring that expired items are removed from the inventory prior to expiration ...
Clinical Research Assistant
New York, NY · On-site
$24 - $30/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Assistant
New York, NY · On-site
$24 - $30/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Assistant
$24 - $29/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Assistant
$24 - $29/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Assistant
New York, NY · On-site
$24 - $29/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Assistant
New York, NY · On-site
$24 - $29/hr
Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with ... Basic understanding of clinical research principles is a plus. * Strong attention to detail ...
Clinical Research Nurse
New York, NY · On-site
$90K - $110K/yr
Key Responsibilities: * IV placement, initiation and management of IV infusions per sponsor ... Previous clinical research experience preferred, but not required * Willingness and ability to ...
Clinical Research Nurse
New York, NY · On-site
$90K - $110K/yr
Key Responsibilities: * IV placement, initiation and management of IV infusions per sponsor ... Previous clinical research experience preferred, but not required * Willingness and ability to ...
Clinical Research Nurse
New York, NY · On-site
$90K - $110K/yr
Key Responsibilities: * IV placement, initiation and management of IV infusions per sponsor ... Previous clinical research experience preferred, but not required * Willingness and ability to ...
Clinical Research Nurse
New York, NY · On-site
$90K - $110K/yr
Key Responsibilities: * IV placement, initiation and management of IV infusions per sponsor ... Previous clinical research experience preferred, but not required * Willingness and ability to ...
Clinical Research Nurse
New York, NY · On-site
$90K - $110K/yr
Key Responsibilities: * IV placement, initiation and management of IV infusions per sponsor ... Previous clinical research experience preferred, but not required * Willingness and ability to ...
Clinical Research Nurse
New York, NY · On-site
$90K - $110K/yr
Key Responsibilities: * IV placement, initiation and management of IV infusions per sponsor ... Previous clinical research experience preferred, but not required * Willingness and ability to ...
Manager Clinical Research Informatics information
See Edison, NJ salary details
$50.7K - $63.9K
3% of jobs
$63.9K - $77.1K
13% of jobs
$82.4K is the 25th percentile. Wages below this are outliers.
$77.1K - $90.3K
22% of jobs
The median wage is $101.4K / yr.
$90.3K - $103.4K
14% of jobs
$103.4K - $116.6K
16% of jobs
$122.3K is the 75th percentile. Wages above this are outliers.
$116.6K - $129.8K
16% of jobs
$129.8K - $143K
7% of jobs
$143K - $156.1K
6% of jobs
$156.1K - $169.3K
2% of jobs
$169.3K - $182.5K
0% of jobs
$182.5K - $195.7K
0% of jobs
$50.7K
$111.1K
$195.7K
How much do manager clinical research informatics jobs pay per year?
What are the most commonly searched types of Clinical Research Informatics jobs in Edison, NJ?
The most popular types of Clinical Research Informatics jobs in Edison, NJ are:
What are popular job titles related to Manager Clinical Research Informatics jobs in Edison, NJ?
For Manager Clinical Research Informatics jobs in Edison, NJ, the most frequently searched job titles are:
- Clinical Research Associate Cro
- Clinical Psychology Research Coordinator
- Part Time Clinical Research Monitor
- Internship Clinical Research Nurse
- Entry Level Clinical Trial Manager
- Clinical Trial Master File Specialist
- Senior Clinical Trial Assistant
- Clinical Research Finance
- Clinical Trials Protocol Administrator
- Assistant Clinical Research Coordinator Ucsf
What job categories do people searching Manager Clinical Research Informatics jobs in Edison, NJ look for?
The top searched job categories for Manager Clinical Research Informatics jobs in Edison, NJ are:
- Clinical Research Assistant
- Clinical Research Associate
- Clinical Research Regulatory Assistant
- Dental Clinical Research Coordinator
- Overnight Clinical Research Coordinator
- Clinical Research Study Manager
- Clinical Trials Coordinator
- Neuroscience Research Coordinator
- Per Diem Clinical Research
- Temporary Clinical Trials Test Subject
What cities near Edison, NJ are hiring for Manager Clinical Research Informatics jobs?
Cities near Edison, NJ with the most Manager Clinical Research Informatics job openings:
Full-time
Medical, Life, Retirement
Re-posted 12 days ago
Abbott rating
7.8
Based on 138 frontline employees who took The Breakroom Quiz
169th of 545 rated manufacturers
Job description
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
Career development with an international company where you can grow the career you dream of.
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
An excellent retirement savings plan with a high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
Our Global Medical & Scientific Affairs Team has an opportunity for a Senior Project Manager, Clinical Research. This role will be located in our Princeton, New Jersey office on site. This role is based in our Abbott Point of Care(APOC) Division. APOC is a global leader in providing critical medical diagnostic and data management products for rapid blood analysis that are intuitive, reliable, and cost-effective. Our i-STAT System is an advanced, portable diagnostic tool that provides real-time, lab-quality results within minutes to accelerate patient-care decision-making. The i-STAT System has the industry's most comprehensive menu of tests in a single, with-patient platform, including tests for blood gases, electrolytes, chemistries, coagulation, hematology, glucose, and cardiac markers. By delivering lab-quality results in minutes, our i-STAT System fosters a collaborative, patient-centered environment while driving improved operational performance.
What You'll Work On
The Senior Project Manager, Clinical Research, will work closely with the Scientific Affairs Manager and Scientific Affairs Director to facilitate cross-functional coordination and ensure the efficient execution, monitoring, and reporting of all Scientific Affairs studies. In addition, they will liaise with cross-functional team members including clinical, regulatory, quality, legal, and supply chain, and will be responsible for managing individual study budgets/milestone payments.
In addition:
Coordinate end-to-end research study operations for Investigator Sponsored Studies (ISS) and Collaborative Research Studies (CRS), including proposal review, contracts, study start-up, material shipments, budget management, and study closeout.
Ensure compliance and audit readiness by maintaining study documentation, conducting investigator/debarment reviews, documenting communications, supporting SOP updates, and maintaining quality system requirements.
Manage financial oversight including Fair Market Value assessments, study budgets, invoice processing, milestone payments, forecasting, and financial tracking/reporting.
Oversee study logistics and site support by coordinating study supplies, regulatory labeling requirements, site instructions, training documentation, and collaboration with R&D, Clinical, Regulatory, and Scientific Affairs teams.
Support Scientific Affairs initiatives including medical education and writing grants, KOL and advisory board contracting, meeting logistics, reporting for review committees, and other activities delegated by Scientific Affairs leadership.
Required Qualifications
Bachelor's degree
10+ years of clinical research/medical affairs/project management experience.
Knowledge and experience in working with clinical trials including investigator-initiated research and collaborative research studies.
Knowledge and experience in oversight of clinical studies, understanding of statistical techniques, tracking clinical studies, and related publications.
Understanding of the clinical laboratory, assay/instrument principles involving in vitro diagnostic products.
Form and develop long-term strategic and professional relationships; display socially and professionally appropriate behavior.
Strong communication skills demonstrated in publications, presentations, etc. including the ability to confidently speak in public, and lead meetings and group discussions.
Ability to work independently and in groups.
Demonstrates leadership skills, initiative, critical thinking, and problem-solving skills.
Strong organization and time management skills
Willing and able to travel up to 10 -15% of the time to meet investigators and clinical trial staff.
Preferred Qualifications
Advanced degree (Master's, PhD, or MD)
Experience with managing publications
Experience running clinical trials in international geographies
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: https://abbottbenefits.com/
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.
The base pay for this position is
$86,700.00 - $173,300.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:Clinical Affairs / StatisticsDIVISION:APOC Point of CareLOCATION:United States > Princeton : 400 College Road EastADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 15 % of the TimeMEDICAL SURVEILLANCE:YesSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment, Keyboard use (greater or equal to 50% of the workday), Work with human blood or other potentially infectious materials, Work with infectious organisms or known infectious materialsAbbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf