Senior Site Contract Manager
Senior Site Contract Manager
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Salary Not Disclosed
1 Vacancy
Job Description
Accountable for the timely preparation and execution of CSAs CDAs and budgets and associated vendor agreements. US this role acts as point person for assigned country / region for legal finance and CDO.
Negotiation of CSAs CDAs other site agreements and Budgets with investigator sites (directly or with support where language necessitates) using appropriate templates guidance and legal/budget playbooks liaising with RD legal for approval to changes not already described.
Provide input for ongoing update of applicable legal and budget playbooks and templates.
Ensure appropriate tracking of CSAs CDAs Country and Site Intelligence and the maintenance of necessary documentation per AbbVie requirements.
Agree manage and communicate regarding priorities with CDO stakeholders legal and finance in alignment with Study and Priority planning. Effectively escalate / communicate to stakeholders and clinical teams in a diplomatic and timely way regarding contract issues that could impact project deliverables.
Lead process improvement projects for the US Contract Management Function and/or be a SME representing the US Contract Management function on process teams with broader impact. Drive for excellence and continuous improvement in delivery of global Contract Management responsibilities.
Demonstrates a high level of applicable competencies in contract management critical thinking highly competent in negotiation and contracting business standards.
Provide guidance to team members within the Contract Management function. May triage and assign workload within the department and mentor/train junior staff members within the work team as requested.
Partner with Country Operations Managers in the countries assigned line reports manage the contracts for to ensure effective and efficient work processes. Ensures any issues are resolved.
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Qualifications :
Bachelors degree or equivalent work experience; a Health Care business legal or scientific discipline preferred.
Significant (at least 5 years) Clinical Research and/or contract/budget experience. Awareness and understanding of compliance and regulatory matters in clinical research. Experience in crossfunctional interactions and working within a global environment an advantage.
Proven negotiation interpersonal and business 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; trackrecord 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 change in the work environment.
Experience in line or matrix management an advantage.
Experience in financial budget cost management/analysis accounting and/or financial planning skills are desirable.
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Key Stakeholders:
R&D Legal Clinical Development Operations Office of Ethics and Compliance Finance Other PSM Functions Global Clinical Trial Sites
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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
