Top 28 Senior clinical research associate Jobs in Somerville Nj

Senior Clinical Trials Management Associate
Kite Pharma —Parsippany-Troy Hills, NJ
- $115,260 - $164,120 a year
- Full-time
- Nursing
- Bachelor of Science
- Data analysis skills
- Health insurance
- Dental insurance
Sr Clinical Research Associate (Sr CRA) - Ophthalmology-Remote
Merck —Rahway, NJ
- $129,000 - $203,100 a year
- Full-time
- Remote
- English
- Microsoft Office
- Driver's License
- Paid holidays
- Health insurance
Senior Clinical Trial Manager
Genmab —Princeton, NJ
- $130,720 - $196,080 a year
- Online Application
- Master's degree
- 8 years
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Senior Manager, Clinical Programming
Genmab —Princeton, NJ
- $131,040 - $196,560 a year
- Online Application
- Computer science
- 6 years
- Computer Science
- Commuter assistance
- Paid parental leave
Senior Project Manager Clinical Research
Abbott Laboratories —Princeton, NJ
- $86,700 - $173,300 a year
- Full-time
- Office
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Tuition reimbursement
Senior Clinical Database Programmer
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Analysis skills
- Quality control
- Mentoring
Quick Apply
Sr. Clinical Trial Associate
Summit Therapeutics —Princeton, NJ
- $117,000 - $137,000 a year
- Office
- Bachelor's degree
- Continuous improvement
Quick Apply
1d
Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
Senior Scientist, Regulatory & Clinical Operations
Hims & Hers —South Plainfield, NJ
- $130,000 - $150,000 a year
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Continuous improvement
- Employee stock purchase plan
- Health insurance
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
Sr Clinical Study Assoc CO
Daiichi Sankyo, Inc. —Basking Ridge, NJ
- $100,960 - $151,440 a year
- Office
- Bachelor's degree
- Travel
Senior Clinical Research Coordinator
Vitalief —New Brunswick, NJ
- $70,000 - $80,000 a year
- Full-time
- Bachelor's degree
- In-person
- Senior level
- Paid holidays
- Disability insurance
Quick Apply
Senior Manager/Associate Director, Clinical Pharmacology
SystImmune —Princeton, NJ
- $150,000 - $200,000 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- Computer skills
Senior Manager, GCP QA
Shionogi Inc. —Florham Park, NJ
- $135,000 - $165,000 a year
- Email
- Hybrid work
- Management
- 5 years
- Bachelor of Science
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
Senior Researchers (Faculty)
Rutgers University —New Brunswick, NJ
- From $156,332 a year
- Email
- Medicine
- University
- Doctor of Philosophy
- Paid holidays
- Dental insurance
Sr. Clinical Trial Manager, Therapeutics and Oncology
Moderna, Inc. —Princeton, NJ
- $130,800 - $209,400 a year
- Full-time
- 5 years
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
Senior Manager, Data Management
Bracco —Princeton, NJ
- Full-time
- 7 years
- English
- Master's degree
Senior Clinical Research Coordinator - Oncology
Vitalief —Newark, NJ
- $75,000 - $85,000 a year
- Full-time
- Hybrid work
- Nursing
- Hospital
- 3 years
- Paid holidays
- Disability insurance
Quick Apply
Senior Director, Clinical Data Management, Therapeutic Area Lead, Melanoma, Hybrid
Merck —Rahway, NJ
- $173,200 - $272,600 a year
- Full-time
- 18 years or older
- Nursing
- 5 years
- Paid holidays
- Health insurance
4d

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Senior Clinical Trials Management Associate

Kite Pharma -
Parsippany-Troy Hills, NJ

Apply Now

Job Details

Full-time
$115,260 - $164,120 a year

Benefits

Health insurance
Dental insurance
Paid time off
Vision insurance
Life insurance

Qualifications

Data analysis skills
ICH guidelines
FDA regulations

Full Job Description

Job Description

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

The Senior Clinical Trials Management Associate is a primarily an in-house sponsor position (although some travel is required) who will oversee multiple aspects of clinical trial conduct including study start-up, document generation and review, tracking of samples enrollment of study participants, and management of vendors.. The candidate must be knowledgeable of clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines. The position will report to a Senior Clinical Trials Manager of Clinical Operations.

Responsibilities include but, are not limited to:

Prepares and/or reviews study-related or essential study start-up documents as they relate to the supported clinical trials as delegated by the study manager (e.g., Clinical protocols, Informed Consent Forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters).
Works with multiple contract research organizations to communicate detailed timelines and ensure that transferred obligations and performance expectations are met. Provides corrective instruction, as necessary, when performance expectations are not being met.
Attends internal team and other meetings as required.
Provides training, as necessary, at investigator meetings and other trial-specific meetings such as site initiation visits and monthly teleconferences.
Creates and reviews site feasibility assessments required for study participation.
Manages and tracks key study deliverables such as screening, enrollment, biological samples and images, data flow and protocol deviations.
Proactively identifies potential study issues/risks and recommends/implements solutions; ensures issues are escalated as appropriate to Senior Manager.
Prepares metrics and updates to key deliverables for management.
Assists in the resolution of clinical trial queries and data review for interim analysis, primary analysis and final database locks.
Prepares site newsletters and other correspondence related to clinical trial conduct (eg, best practices and lessons learned, frequently asked questions) in collaboration with the study team
Assists in resolution of routine study questions from clinical trial sites in adherence to ICH GCP and the study protocol.
May lead less complex studies and/or manage components of more complex studies as a member of the study team
May participate in department initiatives or special projects, such as developing new tools or processes
Ability to coach less experienced colleagues in solving problems
Understands how decisions have an impact to the broader study goals
Other duties as assigned.

Basic Qualifications

BS/BA in nursing, science or health related field and 4 years of related experience – OR -
MS/MA in nursing, science or health related field and 2 years of related experience

Preferred Qualifications

Bachelor’s degree in nursing, science or health related field required with at least five years of related experience. At least three years of clinical trial experience with oncology, hematology or related therapeutic area experience considered a plus
Multiple years of experience managing the work of external candidates
Must be willing to travel at least 25% (possibly more)
Ability to manage time demands, incomplete information or unexpected events
Must display strong analytical and problem solving skills
Attention to detail required
Outstanding organizational skills with the ability to multi-task and prioritize
Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
Working knowledge of transplant patient care and apheresis collection a plus

The salary range for this position is:

Other US Locations: $115,260.00 - $149,160.00.

Bay Area: $126,820.00 - $164,120.00.

Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Apply Now

Refine Your Search

senior clinical research associate jobs in somerville nj

Senior Clinical Trials Management Associate

Sr Clinical Research Associate (Sr CRA) - Ophthalmology-Remote

Senior Clinical Trial Manager

Senior Manager, Clinical Programming

Senior Project Manager Clinical Research

Senior Clinical Database Programmer

Sr. Clinical Trial Associate

Senior Clinical Trial Manager

Senior Scientist, Regulatory & Clinical Operations

Clinical Trial Manager/Senior Clinical Trial Manager

Sr Clinical Study Assoc CO

Senior Clinical Research Coordinator

Senior Manager/Associate Director, Clinical Pharmacology

Senior Manager, GCP QA

Clinical Trial Manager/Senior Clinical Trial Manager

Senior Researchers (Faculty)

Sr. Clinical Trial Manager, Therapeutics and Oncology

Senior Manager, Data Management

Senior Clinical Research Coordinator - Oncology

Senior Director, Clinical Data Management, Therapeutic Area Lead, Melanoma, Hybrid

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