Associate Director, Safety Data Architect

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Job Overview

The Associate Director, Safety Data Architect position at AbbVie is pivotal for individuals who are passionate about enhancing patient safety through diligent analysis and strategic planning. AbbVie is dedicated to discovering and delivering innovative medicines and solutions aimed at addressing significant health issues. The job of a Safety Data Architect involves a combination of clinical development, safety data analysis, and project management, aimed at ensuring the safety and efficacy of AbbVie products.

Company Mission

Founded with the mission to solve crucial health challenges, AbbVie focuses on various therapeutic areas, including immunology, oncology, neuroscience, and eye care. Their commitment is not just about addressing current medical needs but also preparing for future challenges in healthcare. This ethos underpins their work and is reflected in their values of innovation and patient-centric approaches.

Position Responsibilities

The role requires working closely with the clinical trial and patient safety teams to summarize and present safety data from clinical trials. Core responsibilities include:

• Data Management: Functioning as a crucial driver for safety data evaluation to improve presentations and compound safety delivery.
• Coordination: Collaborating with Product Safety Team Leads and Therapeutic Area physicians for data review meetings and deliverables.
• Regulatory Support: Ensuring that safety data contributions align with regulatory submissions and updates to safety monitoring plans.
• Communication: Acting as a communicator between various stakeholders, ensuring consistency and integrity in safety activities across studies.

Qualifications Required

Candidates interested in this position need to meet certain educational and experiential prerequisites:

• Education: A Bachelor’s degree in a healthcare-related field is mandatory; a graduate degree is preferred. Fields of study can include Life Sciences, Pharmacy, Nursing, or other biomedical disciplines.
• Experience: At least 10 years of experience in clinical research within the pharmaceutical industry is essential. This role also requires a solid grasp of the drug development process. Experience in areas like clinical operations, risk management, and drug safety operations will be beneficial.
• Project Management Skills: Expertise in managing cross-functional projects and a clear understanding of clinical trial conduct and scientific strategy is essential.

Skills and Competencies

Additionally, the successful candidate should demonstrate:

• Leadership and Communication Skills: Effective communication of project objectives, issues, and risks are vital to keep teams informed.
• Problem Solving: Ability to navigate conflicts constructively and work collaboratively to foster high-performing teams.
• Quality of Data Analysis: Knowledge of tools and approaches to efficiently assess drug safety.

Work Environment

This role offers the flexibility of being remote from anywhere in the United States, ensuring a comfortable arrangement for the right candidate. It combines independent data analysis with collaborative meetings, emphasizing strong communication skills and teamwork.

Compensation Details

While specific salary information is not explicitly mentioned, AbbVie provides a compensation range based on the job grade at which the position is classified. The individual salary will vary based on multiple factors, including geographic location. The company also notes that this position is eligible for various incentive programs, which can provide additional earnings apart from the base salary.

Benefits

Employees at AbbVie benefit from a comprehensive package which includes:

• Paid time off including vacation, holidays, and sick leave.
• Healthcare options such as medical, dental, and vision insurance.
• A 401(k) plan for retirement savings.
• Opportunities for participation in both short-term and long-term incentive programs.

AbbVie’s Commitment

AbbVie emphasizes diversity and inclusion as integral to its employment practices. The company is an equal opportunity employer, striving to create a community where all qualified candidates can thrive without the hindrance of discrimination based on various protected statuses.

Conclusion

The Associate Director, Safety Data Architect position at AbbVie offers a unique opportunity for experienced professionals in the clinical research domain to impact positively on patient safety through comprehensive data analysis and strategic collaboration. Candidates looking to join a mission-driven organization striving to improve health outcomes globally would find this role particularly rewarding.

This job offer was originally published on himalayas.app