Senior Clinical Site Lead

     

JOB DESCRIPTION:

About Abbott: Abbott is a global healthcare leader dedicated to improving lives through innovative medical solutions. Join us to make a positive impact on the world of clinical research and healthcare.

We are recruiting a Senior Clinical Site Lead (Sr CSL) to be based in Sweden. This key role focuses on driving study execution, site management, and operational excellence while ensuring compliance with all regulations and Abbott’s procedures.

Key Responsibilities:

• Lead site management and study execution throughout all phases of clinical studies.

• Act as the primary contact internally and externally for study sites in Sweden.

• Coordinate clinical studies, from start-up to closeout, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP).

• Develop and maintain productive clinical sites, identifying appropriate investigators and site-specific strategies for patient enrollment.

• Monitor site performance and implement solutions to meet study goals.

• Review and verify data accuracy and completeness from investigational sites.

• Lead compliance activities, including audits, adverse event reporting, and protocol deviation management.

• Provide mentorship to clinical site management team members and support onboarding activities.

• Serve as the EMEA protocol champion for assigned studies, consulting on study design and related activities.

• Collaborate with cross-functional teams, contributing expertise on local regulations and requirements.

Your Profile:

• Background in engineering, science, health science, nursing, or a related field OR equivalent experience in cardiology or clinical research.

• Fluency in English and the local language; additional European language skills are a plus.

• Proficient in MS Office and clinical databases (preferably Oracle).

• Strong self-development skills and ability to work independently.

• Expertise in medical terminology, clinical study conduct, and regulatory compliance (ISO standards, FDA).

• Exceptional communication, organizational, and time management skills.

• Ability to multitask in a fast-paced environment and meet deadlines.

• Team-oriented approach with a constructive attitude.

• Advanced knowledge of clinical and outcomes research study design.

• Willingness to travel up to 70%, including internationally.

Why Abbott: At Abbott, we offer a dynamic environment where innovation and collaboration thrive. You'll have the opportunity to contribute to impactful global clinical studies and grow as a leader in the healthcare industry.

     

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Research and Discovery

     

DIVISION:

MD Medical Devices

        

LOCATION:

Sweden : Remote

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Yes, 75 % of the Time

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Not Applicable