Clinical Trial Contract Manager (On-site/Hybrid)
Boehringer Ingelheim
Ridgefield, CTFull-time
Behavioral Health Market Context
Apply Nowvia Talents By Vaia
Benefits
Health Insurance
Job Description
dgefield, Connecticut site 2-3 times per week typically.
Description
This role will be considered an "On-site/Hybrid" role, which means working from the Ridgefield, Connecticut site 2-3 times per week typically.
The Clinical Trial Contract Manager is responsible for the preparation, negotiation, and administration of a variety of agreements assigned CDA/CTA contract development and negotiations. This role is responsible for the management of the day-to-day operations and oversight with third party contracting negotiator(s) as well as for supporting management goals and objectives of the department.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Duties & Responsibilities
• Prepares, negotiates, and executes a variety of agreements (e.g., master services agreements, confidentiality agreements, Clinical trial agreements, etc.)
• Reviews contract language and prepares responses to negotiate contract modifications
• Supports AD in more complex agreements
• Maintains contract files and systems
• Supports the implementation of contracting-specific and trial metrics and tools to report on, provide visibility into, and analyze performance and deliverables
• Collaboration of third-party contracting negotiator (s) for successful support management of US clinical programs
• Effectively uses evaluation tools and provide oversight over CRO/third party contracting negotiator (s) performance on trial negotiations to address performance issues and ensure high quality deliverables within planned timelines
• Maintains a focused continuous improvement culture by identifying and executing strategies and priorities to enable the Contracting group to deliver value and enhance overall operational effectiveness
• Actively remains current with industry standards, trends, and competitive intelligence on contracting best practices
• Maintains close working relationship with all Clinical Operations as well as Legal, Ethics & Compliance and Clinical Development & Medical Affairs (CDMA)
• Manages the day-to-day operations and assists with oversight with CRO/third party contracting negotiator (s)
• Represents Contracting group for projects and working groups
• Ensures commitment to customer-centric behaviors provides visibility to trial teams and broader Clinical Operations into ongoing work through up-to-date tracking
• Maintains high degree of responsiveness to both internal and external requests
• Resolves issues by working collaboratively across Clinical Operations and other groups within BI
• Assists in delivering appropriate training for the Contracting group in partnership with the Training and Compliance group
Requirements
• Bachelor’s degree from an accredited institution (preferred major/focus: Business/Health Sciences)
• Minimum of five (5) years of relevant experience in contract development and negotiations (preferably in regulated pharmaceuticals or healthcare industry or clinical operations)
• Extensive working knowledge and experience in contract environment, contract negotiation, investigator budgets and or/clinical finance and /or CRO management
• Track record in setting priorities, organization and problem-solving skills which support and enable sound decision making
• Excellent customer service skills and high attention to detail
• Demonstrated analytical skills and critical thinking to resolve issues in a variety of complex situations requiring new solutions
• Experience initiating and leading department and cross-functional strategic initiatives
• Demonstrated experience in the regulated pharmaceutical or healthcare industry
• Thorough understanding of all phases of drug development (I-IV)
• Understanding of federal regulations pertaining to IND and NDA regulations
Eligibility Requirements:
• Must be legally authorized to work in the United States without restriction
• Must be willing to take a drug test and post-offer physical (if required)
• Must be 18 years of age or older
Desired Skills, Experience And Abilities
This position offers a base salary typically between $115,000 and $181,000. The position may be eligible for a role specific variable or performance-based bonus and or other compensation elements. For an overview of our benefits please click here .
Our Company
Why Boehringer Ingelheim?
With us, you can develop your own path in a company with a culture that knows our differences are our strengths \u2013 and break new ground in the drive to make millions of lives better.
Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after \u2013 as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
Want to learn more? Visit https://www.boehringer-ingelheim.com
Seniority level
• Seniority level
Mid-Senior level
Employment type
• Employment type
Full-time
Job function
• Job function
Management and Manufacturing
• Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Boehringer Ingelheim by 2x
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Description
This role will be considered an "On-site/Hybrid" role, which means working from the Ridgefield, Connecticut site 2-3 times per week typically.
The Clinical Trial Contract Manager is responsible for the preparation, negotiation, and administration of a variety of agreements assigned CDA/CTA contract development and negotiations. This role is responsible for the management of the day-to-day operations and oversight with third party contracting negotiator(s) as well as for supporting management goals and objectives of the department.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Duties & Responsibilities
• Prepares, negotiates, and executes a variety of agreements (e.g., master services agreements, confidentiality agreements, Clinical trial agreements, etc.)
• Reviews contract language and prepares responses to negotiate contract modifications
• Supports AD in more complex agreements
• Maintains contract files and systems
• Supports the implementation of contracting-specific and trial metrics and tools to report on, provide visibility into, and analyze performance and deliverables
• Collaboration of third-party contracting negotiator (s) for successful support management of US clinical programs
• Effectively uses evaluation tools and provide oversight over CRO/third party contracting negotiator (s) performance on trial negotiations to address performance issues and ensure high quality deliverables within planned timelines
• Maintains a focused continuous improvement culture by identifying and executing strategies and priorities to enable the Contracting group to deliver value and enhance overall operational effectiveness
• Actively remains current with industry standards, trends, and competitive intelligence on contracting best practices
• Maintains close working relationship with all Clinical Operations as well as Legal, Ethics & Compliance and Clinical Development & Medical Affairs (CDMA)
• Manages the day-to-day operations and assists with oversight with CRO/third party contracting negotiator (s)
• Represents Contracting group for projects and working groups
• Ensures commitment to customer-centric behaviors provides visibility to trial teams and broader Clinical Operations into ongoing work through up-to-date tracking
• Maintains high degree of responsiveness to both internal and external requests
• Resolves issues by working collaboratively across Clinical Operations and other groups within BI
• Assists in delivering appropriate training for the Contracting group in partnership with the Training and Compliance group
Requirements
• Bachelor’s degree from an accredited institution (preferred major/focus: Business/Health Sciences)
• Minimum of five (5) years of relevant experience in contract development and negotiations (preferably in regulated pharmaceuticals or healthcare industry or clinical operations)
• Extensive working knowledge and experience in contract environment, contract negotiation, investigator budgets and or/clinical finance and /or CRO management
• Track record in setting priorities, organization and problem-solving skills which support and enable sound decision making
• Excellent customer service skills and high attention to detail
• Demonstrated analytical skills and critical thinking to resolve issues in a variety of complex situations requiring new solutions
• Experience initiating and leading department and cross-functional strategic initiatives
• Demonstrated experience in the regulated pharmaceutical or healthcare industry
• Thorough understanding of all phases of drug development (I-IV)
• Understanding of federal regulations pertaining to IND and NDA regulations
Eligibility Requirements:
• Must be legally authorized to work in the United States without restriction
• Must be willing to take a drug test and post-offer physical (if required)
• Must be 18 years of age or older
Desired Skills, Experience And Abilities
This position offers a base salary typically between $115,000 and $181,000. The position may be eligible for a role specific variable or performance-based bonus and or other compensation elements. For an overview of our benefits please click here .
Our Company
Why Boehringer Ingelheim?
With us, you can develop your own path in a company with a culture that knows our differences are our strengths \u2013 and break new ground in the drive to make millions of lives better.
Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after \u2013 as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
Want to learn more? Visit https://www.boehringer-ingelheim.com
Seniority level
• Seniority level
Mid-Senior level
Employment type
• Employment type
Full-time
Job function
• Job function
Management and Manufacturing
• Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Boehringer Ingelheim by 2x
Get notified about new Contract Manager jobs in Ridgefield, CT.
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Contract Compliance & Procurement Specialist
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Tarrytown, NY $200,000.00-$250,000.00 4 days ago
Milford, CT $120,000.00-$180,000.00 2 months ago
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Principal Commercial Banking Relationship Manager
Purchase, NY $207,900.00-$431,900.00 1 week ago
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Principal Commercial Banking Relationship Manager
White Plains, NY $130,000.00-$140,000.00 4 days ago
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Technical Project Manager - Electro-Mechanical Systems
Westchester County, NY $215,000.00-$245,000.00 1 week ago
White Plains, NY $90,000.00-$110,000.00 1 week ago
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Qualifications
- •Minimum of five (5) years of relevant experience in contract development and negotiations (preferably in regulated pharmaceuticals or healthcare industry or clinical operations)
- •Extensive working knowledge and experience in contract environment, contract negotiation, investigator budgets and or/clinical finance and /or CRO management
- •Track record in setting priorities, organization and problem-solving skills which support and enable sound decision making
- •Excellent customer service skills and high attention to detail
- •Demonstrated analytical skills and critical thinking to resolve issues in a variety of complex situations requiring new solutions
- •Experience initiating and leading department and cross-functional strategic initiatives
- •Demonstrated experience in the regulated pharmaceutical or healthcare industry
- •Thorough understanding of all phases of drug development (I-IV)
- •Understanding of federal regulations pertaining to IND and NDA regulations
- •Must be legally authorized to work in the United States without restriction
- •Must be willing to take a drug test and post-offer physical (if required)
- •Must be 18 years of age or older
- •Danbury, CT $81,784.00-$106,166.00 4 months ago
- •Senior Associate, Contract and Asset Management
- •Experienced Commercial/Industrial Project Manager
- •Principal Commercial Banking Relationship Manager
- •Senior Associate, Field Management Systems Project Manager and Operations Lead
- •Electrical Project Manager – Control Systems & Panel Design
- •Technical Project Manager - Electro-Mechanical Systems
Benefits
- •Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees
- •This position offers a base salary typically between $115,000 and $181,000
- •The position may be eligible for a role specific variable or performance-based bonus and or other compensation elements
- •Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed
Responsibilities
- •Join to apply for the Clinical Trial Contract Manager (On-site/Hybrid) role at Boehringer Ingelheim
- •This role will be considered an "On-site/Hybrid" role, which means working from the Ridgefield, Connecticut site 2-3 times per week typically
- •This role will be considered an "On-site/Hybrid" role, which means working from the Ridgefield, Connecticut site 2-3 times per week typically
- •The Clinical Trial Contract Manager is responsible for the preparation, negotiation, and administration of a variety of agreements assigned CDA/CTA contract development and negotiations
- •This role is responsible for the management of the day-to-day operations and oversight with third party contracting negotiator(s) as well as for supporting management goals and objectives of the department
- •As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers
- •Prepares, negotiates, and executes a variety of agreements (e.g., master services agreements, confidentiality agreements, Clinical trial agreements, etc.)
- •Reviews contract language and prepares responses to negotiate contract modifications
- •Supports AD in more complex agreements
- •Maintains contract files and systems
- •Supports the implementation of contracting-specific and trial metrics and tools to report on, provide visibility into, and analyze performance and deliverables
- •Collaboration of third-party contracting negotiator (s) for successful support management of US clinical programs
- •Effectively uses evaluation tools and provide oversight over CRO/third party contracting negotiator (s) performance on trial negotiations to address performance issues and ensure high quality deliverables within planned timelines
- •Maintains a focused continuous improvement culture by identifying and executing strategies and priorities to enable the Contracting group to deliver value and enhance overall operational effectiveness
- •Actively remains current with industry standards, trends, and competitive intelligence on contracting best practices
- •Maintains close working relationship with all Clinical Operations as well as Legal, Ethics & Compliance and Clinical Development & Medical Affairs (CDMA)
- •Manages the day-to-day operations and assists with oversight with CRO/third party contracting negotiator (s)
- •Represents Contracting group for projects and working groups
- •Ensures commitment to customer-centric behaviors provides visibility to trial teams and broader Clinical Operations into ongoing work through up-to-date tracking
- •Maintains high degree of responsiveness to both internal and external requests
- •Resolves issues by working collaboratively across Clinical Operations and other groups within BI
- •Assists in delivering appropriate training for the Contracting group in partnership with the Training and Compliance group
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