Clinical Research Specialist

2 weeks ago

Burlington, Massachusetts, United States Abbott Full time

About Abbott
Abbott is a leading global healthcare organization dedicated to enhancing the quality of life for individuals at every stage of their health journey. Our extensive portfolio includes innovative technologies across various healthcare sectors, including diagnostics, medical devices, nutritionals, and branded generic medicines.

Heart Failure Division
Within Abbott's Heart Failure division, we are focused on developing advanced solutions for the diagnosis, monitoring, and management of heart failure, empowering individuals to regain their health and continue their lives.

Position Overview
The Clinical Research Scientist plays a crucial role in our expanding clinical affairs team. This position is responsible for authoring scientific documentation related to the design, execution, and reporting of clinical trials specifically in the area of Heart Failure, with an emphasis on mechanical circulatory support and hemodynamic monitoring.

Key Responsibilities
This role will:

  • Produce scientific materials necessary for the planning and execution of clinical trials, including but not limited to: clinical trial protocols, case report forms, informed consent documents, prior investigation reports, and investigator brochures.
  • Contribute as an author to peer-reviewed publications of clinical study findings, collaborating with investigator authors and project management.
  • Develop presentations to share clinical data at major international conferences.
  • Work closely with statistics, medical affairs, and regulatory affairs teams to meet business objectives as defined by marketing and reimbursement needs.
  • Synthesize literature across various products and therapies within the designated therapeutic area.
  • Engage with external stakeholders, including physician investigators and key opinion leaders, representing Abbott as a scientific authority in the assigned therapy.
  • Draft documents to support regulatory submissions for Abbott products and address inquiries from regulatory bodies regarding existing submissions.

Qualifications
To be considered for this position, candidates should possess:

  • A PhD in biomedical engineering, biological sciences, biostatistics, or a related discipline.
  • Familiarity with mechanical circulatory support technologies, heart failure pathophysiology, echocardiography, cardiovascular hemodynamics, or heart failure medicine is preferred.
  • Experience in data analytics is advantageous.
  • A proven ability to independently solve problems.
  • Capability to work effectively both as part of a team and as an individual contributor in a dynamic environment.
  • Strong organizational skills and self-motivation to initiate and complete tasks.

Essential Attributes
Successful candidates will demonstrate:

  • Collaborative working style, both internally and externally.
  • Ability to manage and prioritize multiple tasks while adapting to a fast-paced environment.
  • Effective communication skills with cross-functional teams.
  • Excellent oral and written communication abilities.
  • Highly analytical mindset.
  • Strong interpersonal skills, including influencing, negotiation, and teamwork.

Working at Abbott
At Abbott, you will have the opportunity to engage in meaningful work, develop your career, and enjoy a fulfilling life.

Benefits
Employees have access to a range of benefits, including:

  • Career development opportunities within a global organization.
  • Comprehensive medical coverage through the Health Investment Plan (HIP) PPO.
  • A robust retirement savings plan with significant employer contributions.
  • Tuition reimbursement and educational benefits for pursuing higher education.
  • A workplace recognized for its commitment to diversity and inclusion.

The compensation for this role is competitive and varies based on location and experience.

Abbott is an Equal Opportunity Employer, committed to fostering a diverse workforce and providing reasonable accommodations for qualified individuals with disabilities.

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