Senior Contract Management Specialist
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What you'll do
- Accountable for the timely preparation and execution of CDAs, CSAs and budgets and related vendor agreements and point person for their country / region for legal, finance, Site Management and CPD.
- The SnrCMS will be responsible and/or have oversight for more than one country and/or a Small Business Unit (SBU)
- Negotiation of CDAs, CSAs and Budgets with investigator sites (directly of with support from local monitor where language necessitates), using templates, guidance and legal/budget playbooks, liaising with R+D legal for approval to changes not already described
- Input into legal aspects of Informed Consents, to ensure first pass acceptance or rapid resolution of issues using legal playbook/guidance and/or consulting R+D legal as necessary
- Ensure input is provided for ongoing update of legal and budget playbooks and templates for the countries in their area of responsibility
- Ensure appropriate tracking of CDAs, CSAs, Site Intelligence, KPIs and Metrics.
- Set, manage and communicate priorities to local affiliate stakeholders, legal and finance in alignment with Study plans and priority for start-up.
- Lead process improvement projects for the OUS Contract Management Function and/or be a Subject Matter Expert representing the OUS Contract Management function on process teams with broader impact
- Take on functional responsibility as a “Therapeutic Area Captain” for the global Contract Management function; fostering consistency, SMM alignment and white glove service to internal stakeholders in the relevant TA
- Line management of CMSs / CMAs employees within the Contract Management function.
- Drive for excellence and continuous improvement in delivery of global Contract Management responsibilities, by example and influence within the Contract Management function.
What they're looking for
- Bachelor’s degree or equivalent tertiary qualification; a Health Care, legal or scientific discipline preferred.
- Significant Clinical Research and contract/budget experience.
- Awareness and understanding of compliance and regulatory matters in clinical research.
- Proven negotiation, tact and diplomacy skills.
- Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities.
- Sense of urgency and strong goal orientation; track-record of meeting deadlines and goals.
- Strong written and verbal communication including written and verbal fluency in English and local language (if not English) and interpersonal skills, including conflict resolution and problem solving.
- Proactive and positive team player. Able to maintain high performance during times of ambiguity and changes in the work environment.
Nice to have
- Experience in cross-functional interactions and working within a global environment an advantage.
- Experience in line or matrix management an advantage.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Reporting the Clinical Site Contracting & Engagement Manager
Position Overview:
The Senior Contract Management Specialist (SnrCMS) is responsible for ensuring the timely and appropriate execution of Confidentiality Disclosure Agreements (CDAs), Clinical Study Agreements (CSAs), associated Budgets, and vendor agreements in their country(ies) / region of responsibility. The SnrCMS functions as a senior person within the organisation, being the SME for global topics and driving excellence, improvement projects and the development of functional tools and being a example to less experienced colleagues.
Highlighted Responsibilities:
- Accountable for the timely preparation and execution of CDAs, CSAs and budgets and related vendor agreements and point person for their country / region for legal, finance, Site Management and CPD.
- The SnrCMS will be responsible and/or have oversight for more than one country and/or a Small Business Unit (SBU)
- Negotiation of CDAs, CSAs and Budgets with investigator sites (directly of with support from local monitor where language necessitates), using templates, guidance and legal/budget playbooks, liaising with R+D legal for approval to changes not already described
- Input into legal aspects of Informed Consents, to ensure first pass acceptance or rapid resolution of issues using legal playbook/guidance and/or consulting R+D legal as necessary
- Ensure input is provided for ongoing update of legal and budget playbooks and templates for the countries in their area of responsibility
- Ensure appropriate tracking of CDAs, CSAs, Site Intelligence, KPIs and Metrics.
- Set, manage and communicate priorities to local affiliate stakeholders, legal and finance in alignment with Study plans and priority for start-up.
- Lead process improvement projects for the OUS Contract Management Function and/or be a Subject Matter Expert representing the OUS Contract Management function on process teams with broader impact
Take on functional responsibility as a “Therapeutic Area Captain” for the global Contract - Management function; fostering consistency, SMM alignment and white glove service to internal stakeholders in the relevant TA
- Line management of CMSs / CMAs employees within the Contract Management function.
- Drive for excellence and continuous improvement in delivery of global Contract Management responsibilities, by example and influence within the Contract Management function.
Qualifications
- Bachelor’s degree or equivalent tertiary qualification; a Health Care, legal or scientific discipline preferred.
- Significant Clinical Research and contract/budget experience. Awareness and understanding of compliance and regulatory matters in clinical research. Experience in cross-functional interactions and working within a global environment an advantage.
- Proven negotiation, tact and diplomacy skills.
- Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities.
- Sense of urgency and strong goal orientation; track-record of meeting deadlines and goals.
- Experience in line or matrix management an advantage.
- Strong written and verbal communication including written and verbal fluency in English and local language (if not English) and interpersonal skills, including conflict resolution and problem solving.
- Proactive and positive team player. Able to maintain high performance during times of ambiguity and changes in the work environment.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Company
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