Instagram
youtube
Facebook

Senior Clinical Site Lead - Dallas/Fort Worth, Tx

6+ years
$75,300.00 – $150,700.00
10 March 10, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Clinical Site Lead - Dallas/Fort Worth, TX

About Abbott:
Abbott is a global healthcare leader dedicated to improving lives with breakthrough science and technology. With a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines, Abbott serves people in over 160 countries.

Working at Abbott:
At Abbott, employees have access to career development opportunities, comprehensive health and wellness programs, tuition reimbursement, and an excellent retirement savings plan. The company has been recognized as one of the best places to work for diversity, working mothers, female executives, and scientists.

The Opportunity:
The Senior Clinical Site Lead for the Dallas/Fort Worth, TX region is responsible for driving study execution and operational excellence across Abbott Cardiovascular therapies. This role involves protocol execution, clinical trial enrollment, data collection, and adherence to ICH-GCP and clinical research standards.

Responsibilities:
Develop and maintain a productive clinical territory:

  • Identify, develop, and maintain clinical sites.
  • Assess investigators’ interests and qualifications.
  • Maintain open communication with key site personnel.
  • Provide ongoing technical support to customers and field staff.
  • Facilitate communication between clinical sites and Abbott staff.

Manage all aspects of study lifecycle:

  • Facilitate site nomination, qualification, and startup processes.
  • Train facility staff regarding protocol requirements and technology.
  • Develop site-specific strategies to promote patient enrollment.
  • Monitor compliance with regulatory and legal requirements.
  • Ensure adherence to study goals and protocol execution.

Regulatory and Quality Compliance:

  • Develop strategies to avoid deviations and educate sites on compliance tools.
  • Ensure accurate data collection, review adverse events, and resolve discrepancies.
  • Maintain accurate records of monitoring visits and site performance.
  • Provide timely feedback and escalate non-compliance when necessary.

Training and Procedure Coverage:

  • Train site and Abbott staff on clinical trials and commercial product launches.
  • Provide clinical and technical expertise for study procedures.
  • Attend study procedures and follow-ups as needed.

Territory Optimization and Clinical Expertise:

  • Enhance site capabilities to take on complex trials.
  • Communicate study updates and best practices.
  • Contribute to protocol development and study execution feedback.
  • Act as a mentor to site management staff.

Collaboration with Commercial Partners:

  • Educate sales teams and customers on Abbott products.
  • Support customers with technical questions and troubleshooting.
  • Strengthen relationships with key clients and stakeholders.

Qualifications:
Required:

  • Bachelor’s degree in biological sciences, engineering, or clinical research experience (8-9 years).
  • Minimum of 6 years of relevant professional experience, including:
    • 2-3 years in Clinical Research.
    • 3-4 years in Laboratory (hospital, research, or industry) OR 1-2 years in Quality Assurance OR 1-2 years in Customer Contact.
  • Strong verbal and written communication skills.
  • Proficiency in MS Office Suite.

Preferred:

  • Master’s degree.
  • Competency in catheterization lab and operating room protocols.
  • Medical Technology MT(ASCP) certification or equivalent.
  • 10 years of clinical trial experience in the cardiovascular field.
  • Ability to analyze data and provide strategic solutions.

Compensation:
Base pay range: $75,300.00 – $150,700.00 (pay may vary based on location).

Apply Now:
Learn more about Abbott’s health and wellness benefits at
www.abbottbenefits.com. Abbott is an Equal Opportunity Employer committed to diversity.

Connect with us: