Sr Clinical Contract Specialist Jobs

Minimal 2 years in contract operations, contract management, or comparable experience.

Partner with IT to continuously improve contracting management platform, lead user testing and user communications.

B.S./B.A in Engineering, Finance, Business

Experience and proficiency with contracting system and platform is a must

Experience in large, complex data migration is a must

Partner with Business Analytics to ensure 100% of contract data is ready-to-use and reportable.

Demonstrates effective time management skills; able to independently prioritize multiple tasks.

Elevates to CTA Lead role for portfolio management for sponsor satisfaction.

Shows a commitment to and demonstrates the ability to consistently perform high quality work with minimal management oversight.

Understands the clinical contract process, project management and service delivery.

Enhances skill at discerning and responding to issues at sites that pose risk and escalating accordingly.

Clinical Trial Contracts and clinical budgets negotiations experience with clinical sites Required.

Document quality issues and performance measures for management review

Ensure compliance and understanding of quality requirements

Manage special projects and make recommendations as appropriate

Perform other duties and responsibilities as assigned

Excellent computer and presentation skills

Strong business development, organization, analytical and problem-solving skills

Experience in Care Delivery, Care Coordination, or Business Intelligence for either Skilled Nursing, or Senior Living facilities

Effectively use and search the knowledge base, consistently contributing new or updated superior quality content

Enhance, advocate, and exemplify KCS methodologies in addition to authoring and updating knowledgebase content

Mentor less experienced team members on trouble shooting SaaS products, customer support best practices, and internal processes

Formalized approach to problem-solving, certification in RCA an asset

Excellent communication skills, written and oral with acumen for conveying complex concepts to a variety of audiences

2 – 5 years of relevant experience performing comparable duties and responsibilities with international/aerospace/defense contracting

Membership/involvement in National Contract Management Association (NCMA) desired

Monitors and administers the business provisions of assigned contracts to ensure that contract requirements are met.

Prepares letters to clients notifying them of contract cost limitations and requirements for additional funds.

Furnishes business and financial information requested by the client, as delegated by the Project Manager.

Performs other responsibilities associated with this position as may be appropriate.

Clinical Trial Manager position open for a biotechnology sponsor company

This position is 100 % REMOTE and Rates ARE VERY FLEXIBLE ***

The Sr. Clinical Trial Manager is responsible for the routine cross-functional operations of assigned studies.

● Manages the implementation, on-time execution and conduct of clinical studies.

● Manage the development of study plans, timelines, vendor selection as well as ensuring quality and compliance

● Ability to manage delegated aspects of assigned clinical trials

Clinical and product management experience that is customer focused (RN preferred)

Translate customer needs into functional requirements that drives action and provides sound direction to engineering, product owners and stakeholders

Develop and manage strong, collaborative relationships with associated product team and other stakeholders, as needed, to help drive results

Collaborate without cross-functional partners in operations, engineering, analytics, customer success, product and legal.

Collaborate with other VCS product owners on user stories and ensure cross team communication, outlining key dependencies and surfacing any risks.

Identify and evaluate activities that prioritize process improvements or gaps

Assist with essential documents collection, review and archiving (TMF management)

Provide project management support for PTX project team, including vendor oversight

Conduct Site Initiation, Routine, and Close-out monitoring site visits, either on-site or remotely, prepare visit correspondence and records including trip reports

Oversee the conduct of assigned study sites, including ensuring compliance with SOPs, federal and local regulations, and ICH and GCP guidelines

Assist in the review and /or development of clinical trial documents such as study plans and training materials

Participate in and assist with facilitation of project team meetings

Clinical Trial Manager position open for a small-mid sized CRO company.

This position is 100 % REMOTE and Rates ARE VERY FLEXIBLE ***

The Sr. Clinical Trial Manager is responsible for the routine cross-functional operations of assigned studies.

● Manages the implementation, on-time execution and conduct of clinical studies.

● Manage the development of study plans, timelines, vendor selection as well as ensuring quality and compliance

● Ability to manage delegated aspects of assigned clinical trials

Manages, tracks, and monitors the electronic signature and contract management system uploading processes across the group

Schedules and coordinates meetings, helps prepare agendas, presentation material, and minutes for specified meetings

Compiles and collates data for assessments and the development of intelligence dashboards

Ensures scheduled SB&C reports are received, complete, and accurate

Assists Site Budgets Leads (SBLs) with investigator grant, site-facing budget, budget escalation trackers, and other deliverables

Assist Site Contracts Leads (SCLs) with letters, contract amendments, and other documents

Location: 100% Remote- must be willing to work EST Time Zone

any other skill set is added bonus

Extensive Cerner Build Experience- Required

Job Type: Full Time / Permanent

Work Authorization: No C2C or Sponsorship

Build in CCL Rules Development 70% and Adhoc 30%

Job Title: Sr. Specialist, Contract Management

Advises internal clients concerning legal and contractual requirements and enforces L3Harris’ objectives and standards in coordination with business leadership.

UCC and international commercial contract law knowledge.

Experience in negotiation and long-term administration of commercial contracts

Maximizes profit and cash flow while minimizing risk in the negotiation of contracts.

Champions integrity and ethical behavior and is alert to potentially difficult situations and proactively provides guidance as needed.

Effectively use and search the knowledge base, consistently contributing new or updated superior quality content

Enhance, advocate, and exemplify KCS methodologies in addition to authoring and updating knowledgebase content

Mentor less experienced team members on trouble shooting SaaS products, customer support best practices, and internal processes

Formalized approach to problem-solving, certification in RCA an asset

Excellent communication skills, written and oral with acumen for conveying complex concepts to a variety of audiences

Demonstrated ability to multi-task, prioritize, and manage customer expectations

Support administration activities of clinical systems (e.g., User Management).

Experience in developing business specifications/requirements and user acceptance testing for computer systems.

Background of SAS programming or Data Management for clinical trials preferred

Good organization skills, ability to manage multiple tasks.

Work with end users and SMEs to define clinical data visualization business requirements and data elements

Experience with Tibco Spotfire (dashboard, visualization & report development) or other data review tools.

Clinical Trial Manager position open for a small-mid sized CRO company.

This position is 100 % REMOTE and Rates ARE VERY FLEXIBLE ***

The Sr. Clinical Trial Manager is responsible for the routine cross-functional operations of assigned studies.

● Manages the implementation, on-time execution and conduct of clinical studies.

● Manage the development of study plans, timelines, vendor selection as well as ensuring quality and compliance

● Ability to manage delegated aspects of assigned clinical trials

Clinical Trial Manager position open for a small-mid sized CRO company.

This position is 100 % REMOTE and Rates ARE VERY FLEXIBLE ***

The Sr. Clinical Trial Manager is responsible for the routine cross-functional operations of assigned studies.

● Manages the implementation, on-time execution and conduct of clinical studies.

● Manage the development of study plans, timelines, vendor selection as well as ensuring quality and compliance

● Ability to manage delegated aspects of assigned clinical trials

Clinical Trial Manager position open for a small-mid sized CRO company.

This position is 100 % REMOTE and Rates ARE VERY FLEXIBLE ***

The Sr. Clinical Trial Manager is responsible for the routine cross-functional operations of assigned studies.

● Manages the implementation, on-time execution and conduct of clinical studies.

● Manage the development of study plans, timelines, vendor selection as well as ensuring quality and compliance

● Ability to manage delegated aspects of assigned clinical trials

· National Contract Management Association (NCMA) membership desired

· Bachelor’s degree and 5+ years of federal contracts experience

· Professional certification (i.e. CFCM, CCCM, CPCM) is desired

· Prepare, organize and maintain contract records and files documenting contract performance and compliance

· Review and negotiate non-disclosure agreements, teaming agreements, subcontractor documents with prime/RFQ flow-down clauses with minimal oversight

· Prepare and perform Contract Kick Off Meetings

Assist in developing action plans and strategies for addressing deficiencies in partnership with operations management

Direct the implementation of training materials/revisions from the national education team

Identify and communicate professional development needs across the region and ensure a continuing clinical education program is in place

Ensure all new and existing clinics exceed state/federal requirements

An Advanced Degree in related field is required/or willingness to pursue or equivalent experience.

Strong communication skills, both written and oral