Live opening · Posted 5 days ago

Director, Medical Affairs (m/f/d)

Abbott India Limited · 3 Locations
Workday
You are 5 days behind. JobBeeper subscribers saw this role while it was still new.

At a glance

The key details from the original listing.

Posted 5 days ago
CompanyAbbott India Limited
Location3 Locations
SourceWorkday
Listed5 days ago

Your early-applicant advantage

Live timing from JobBeeper.

Live data
0 min from Workday publishing this role to us finding it
6 min median time from a role going live to a subscriber being told
6 hours subscribers had this role before this page existed
16,371 roles found in the last 24 hours — the newest are not on this site yet
Start your free trial →

About the role

Description supplied by the original job listing.

JOB DESCRIPTION:
Director Global Medical Affairs - Heart Failure (m/f/d)
Abbott – Heart Failure Division
Abbott’s Heart Failure business is expanding its Global Medical Affairs organization, and we are seeking an experienced Director, Global Medical Affairs to help shape the future of mechanical circulatory support and hemodynamic management worldwide.
This strategic leadership role reports directly to the Chief Medical Officer / Divisional Vice President, Global Medical Affairs and will be based in Europe.
Why This Role Matters
This is a high‑impact position at the forefront of advancing innovative therapies for patients living with heart failure. The Director will play a key role in guiding the clinical and scientific strategy across a rapidly evolving portfolio, partnering closely with Clinical Affairs, R&D, Market Access, Marketing, and Commercial teams.
The role requires a significant global presence (approx. 60% travel) to engage with investigators, clinical sites, and internal stakeholders.
This position will manage Clinical Research professionals to provide medical guidance for the business group, including support to maintain focus on product performance and safety, ISS, grants, and scientific activities. In addition, Director will work cross functionally to support the review, implementation and publication of clinical trial results. This role provides input to establish the range plans and goals for clinical science, and is responsible for the implementation and maintenance of the clinical research-related policies, processes and procedures related to their respective functional areas.
Director provides leadership and direction to product performance testing and evaluation, use clinical and medical experience and knowledge in the area of clinical research, and safety to direct risk management activities, and serves as an advisor to Clinical Affairs to support publications, abstracts and presentation of clinical research. Ensures critical input to establish and implement required product safety processes and procedures for new products and technologies as clinical studies are implemented, worldwide regulatory approvals are obtained and new products are commercialized.
Key responsibilities
Regionally responsible for Investigator Initiated Study and Research Grant programs
Develop the priorities for the Global Abbott HF ISS strategy
Responsible for medical affairs contributions to physician level professional education on advanced HF, MCS and hemodynamic management
Work with professional societies on increasing awareness and knowledge about advanced HF and hemodynamic management
Assists the commercial and marketing teams with strategic customer and KOL interactions as needed.
Leads and delivers internal educational activities related to HF
Provide input to R&D on all aspects and stages of the product portfolio
Support clinical affairs and help drive Abbott led trials and ensure the region is represented in critical evidence generation in the field of HF.
Be responsible for off label discussions with clinicians in the OUS region.
Assist market access with clinical input to reimbursement processes OUS
Represent Abbott HF Medical Affairs in interactions with regulatory bodies
Assists investigation teams by providing medical input as needed.
Provides medical support for reporting to regulatory authorities when needed.
Responsible for updating medical affairs procedural documents and submitting change requests when needed.
Key Requirements
MD degree (+ 8 years) with clinical experience in the cardiovascular disease area
Applicants with documented medical or surgical experience treating patients with advanced heart failure will be preferred
Experience with medical research and scientific publishing required.
Industry experience preferred but not required.
Fluent English required, any additional language is a plus
Apply today, join Abbott and Do Work That Matters
The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:Medical & Scientific Affairs
DIVISION:HF Heart Failure
LOCATION:Spain : Remote
ADDITIONAL LOCATIONS:Germany > Hesse : Helfmann - Park 7, Sweden : Remote
WORK SHIFT:Standard
TRAVEL:Yes, 50 % of the Time
MEDICAL SURVEILLANCE:Not Applicable
SIGNIFICANT WORK ACTIVITIES:Not Applicable

Get JobBeeper Mobile App

Never miss a job opening! Get instant job alerts on your phone.

Subscribers see fresh openings within minutes. Download the JobBeeper App on Google Play to get real-time push notifications and apply before anyone else.

⚡ Instant Push Alerts 🎯 Tailored Filters 🚀 Direct Employer Links
GET IT ON Google Play

More openings worth a look

Recently tracked roles with full details and direct application links.

6 roles
Good roles move before most people even see them. Tell JobBeeper what you want and get fresh matches delivered in minutes.
Start your free trial →
⚡ Get fresh job alerts 📱 Get App