Company Description
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 immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description
Manages/oversees site/country or district related activities as they relate to AbbVie clinical studies (e.g. country feasibility, site evaluation/selection and activation, contracts/budget negotiation, regulatory/EC submissions startup, issue management, relationship management, monitoring, site closure). Accountable for the on-time and within budget execution of all clinical trials within a Country/District(s). Provide local regulatory and legal requirement expertise.
- Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Monitor regulatory reforms and industry trends within country / region. Conduct and/or implement impact analysis of all significant changes to conform with updated regulatory / industry regulations affecting conduct of clinical studies.
- Ensures audit and inspection-readiness at all times. Country contact for regulatory agency questions related to monitoring processes and procedures. Drive CAPA preparation and implementation.
- Accountable for managing country/district resources including need identification, timely hiring and allocation, and managing changes to hiring plan. Responsible for staff recruitment and retention plans.
- Accountable for functional budget planning and administration.
- Provide leadership to the Country/District and be accountable for growth and development of a world class workforce that role models AbbVie behaviors.
- Drives a learning environment and ensures continuous improvement in Country/District(s)
performance by using innovative approaches, active analysis of Key Performance Indicators,
metrics and milestones. Driving simplicity in process and approach, and enhancing agility.
- Accountable for ensuring SITE M&M leadership, collaboration and teamwork across all key stakeholders within the Country(s).
- May lead global Task Forces and Initiatives. Interacts with peers within the industry to stay
abreast of regulatory landscape, raise AbbVie's profile in the R&D community. Accountable for
driving affiliate R&D Community goals in partnership with GMA
Qualifications PREFERRED QUALIFICATIONS:
- Education: Bachelors or equivalent degree, health related (e.g. Medical, Scientific, Nursing,
Pharmacy) preferred.
- Site Monitoring Experience: Minimum 3 years. Preferably having monitored and/or managed a
study within a Country from start to close.
- Experience in functional budget planning, resource planning & assignment, quality management in a Country lead capacity preferred.
- At least 2 years of experience in line management of staff including acquisition of talent,
performance management, growth and development, managing employee relations, coaching and mentoring of staff and teams preferred.
- Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making.
- Excellent interpersonal skills with the ability to communicate persuasively and with clarity,
flexibility and adaptability to changing requirements, resourcefulness and creativity. Demonstrated proactive and positive team player.
- Exhibits strong planning and organizational skills and high level of flexibility in a dynamic
environment with experience leading (within country or region) projects with competing deadlines;
- Experience across multiple Therapeutic Areas and Study Phases.
- Demonstrating business ethics and integrity Code of Conduct & Business Integrity
AbbVie is committed to observe high integrity and ethical standards in all its business dealings with our customers, with each other, business partners and suppliers.
AbbVie as a responsible corporate citizen will adhere to these standards, as well as to local, national and international laws.
All AbbVie employees are responsible for maintaining the Company's reputation for conduct in accordance with the highest level of business integrity, ethics and compliance with the law. Soliciting and/or accepting/attempting/offering bribes or any illegal gratification is therefore cause for immediate dismissal.
Candidate is therefore required to maintain the highest ethical standards in his conduct of Company affairs at
all times and up hold the AbbVie Values.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
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
