Senior Clinical Publications Manager - EP Devices

RXinsider LTD.; Plymouth (MN); On-site; USD 113,000 - 227,000; Full time

Benefits offered by this job

Tuition reimbursement

401(k) retirement with company match

Health care and well-being programs

Paid time off

Job summary

Abbott, a global healthcare leader, seeks a Sr. Clinical Publication Manager for its Electrophysiology unit in Minnesota.

You will design and execute publication plans for in-human device data, leading medical writers and partnering with clinical, regulatory, and marketing teams to translate trial findings into peer‑reviewed manuscripts and conference materials. Responsibilities include strategic planning, timelines, and ensuring compliant publication practices under GPP and ICMJE guidelines.

Qualifications

• Advanced degree in life sciences or related field.
• 5–7+ years in medical publications or medical communications.
• Strong background in cardiology, medical devices, or cardiac electrophysiology.
• Expert knowledge of clinical trial designs and statistical methodologies.

Responsibilities

• Design and deliver the scientific publication plan for in-human electrophysiology device data.
• Lead a team of medical writers and collaborate with cross-functional partners and external stakeholders to translate complex clinical trial findings into peer‑reviewed manuscripts and congress presentations.
• Develop and execute global publication plans in Electrophysiology, ensuring timely, ethical, and compliant publication of data.
• Coordinate abstracts, posters, and podium presentations; review documents for clinical accuracy; manage external medical agencies.

Skills

Clinical trial design

Statistical methods

Medical communications

Cardiology knowledge

Education

PhD / PharmD / MD / Master’s in biosciences

Job description

Abbott, a global healthcare leader, seeks a Sr. Clinical Publication Manager for its Electrophysiology unit in Minnesota.

You will design and execute publication plans for in-human device data, leading medical writers and partnering with clinical, regulatory, and marketing teams to translate trial findings into peer‑reviewed manuscripts and conference materials. Responsibilities include strategic planning, timelines, and ensuring compliant publication practices under GPP and ICMJE guidelines.