Alcon

Sr. Global Program Safety Team Lead - Oncology

Alcon$248K — $461K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Medical Degree or equivalent required; PhD, PharmD preferred
  • Minimum 5 years of clinical experience postdoctoral
  • At least 7 years of progressive drug development experience, including 5 years in a global context
  • Solid preparation experience for clinical safety assessments and regulatory submissions
  • Substantial experience in leading cross-functional, multicultural teams
  • Strong experience in safety issue management
  • Extensive expertise in drug development, clinical methodology, and regulatory requirements

Responsibilities

  • Manage disease area within the Medical Safety organization to support robust Benefit-Risk evaluations
  • Enhance the training and performance of Medical Safety physicians and scientists
  • Provide expert safety input to clinical development programs
  • Oversee safety signal detection, monitoring, and management
  • Document and track medical safety activities and regulatory responses
  • Lead the development of safety strategy for health authority responses
  • Contribute to departmental goals and objectives

Benefits

  • Health, life, and disability benefits
  • 401(k) with company contribution and match
  • Generous time off package including vacation and personal days
  • Performance-based cash incentives and eligibility for annual equity awards
Full Job Description
Job Description Summary
Join us in a high-impact leadership role at the forefront of Oncology drug development.

As Senior Global Program Safety Team Lead, you will bring clinical insight, strategic thinking, and strong leadership to complex safety decisions, helping shape development pathways and advance medicines that could change patients' lives.

Job Description

Key Responsibilities
  • Manage an efficient and successful disease area within the Therapeutic Area (TA)/Development Unit (DU) Medical Safety organization, which provides robust medical and science-driven contribution to BenefitRisk evaluation throughout product lifecycle to enable Novartis to provide impactful medicines to patients worldwide
  • Enhance scientific and clinical experience of Medical Safety physicians / scientists through continuous training and coaching. Prepares safety objectives and evaluates and manages performance of the Medical Safety associates within the TA/DU. Identifies talents and high potential associates and is able to defend and discuss in front of leadership team. Together with associates identifies carrier development opportunities and support associates in the carrier path
  • Provide expert safety input to the clinical development program for assigned projects/products and be an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT) -Is responsible for safety issue management from formation of Global Program Team (GPT) through Life Cycle Management
  • Responsible for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information, based on information from all relevant line functions, post-marketing data, and other sources
  • Responsible for documentation/tracking/record keeping of the assigned compounds medical safety activities and for responses to inquiries from regulatory authorities or health care professionals on safety issues
  • Leading the preparation of the safety strategy for health authority responses and strategy, in collaboration with other project team members
  • Contribute to and often leading the development of departmental and functional/business unit goals and objective


Essential Requirements
  • Medical Degree or equivalent (preferred), PhD, PharmD or equivalent graduate level health care professional degree required. Specialty Board certification desirable
  • Minimum 5 years clinical experience postdoctoral
  • At least 7 years progressive experience in drug development in a major pharmaceutical company (of which 5 years in a global position), including 5 years in safety at a medical position
  • Solid expertise in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information - to include NDA submission documents
  • Substantial experience in leading cross-functional, multicultural teams
  • Strong experience with (safety or others) issue management
  • Extensive experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publication
  • Strong leadership skills including coaching; motivating and directing, and fostering teamwork. Ability to develop and maintain effective working relationships with subordinates, superiors and peers


Languages:
  • Fluent English (both spoken & written) is required. Additional languages are an advantage.


Beneficial skills and knowledge:
  • Post graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent)
  • Strong negotiation and conflict management skills
  • Strong experience with medical writing and delivering high quality documents such as RMPs, PSURs


This is your opportunity to lead at the forefront of Oncology development and influence the future of patient safety on a global scale. Apply now to join Novartis and help bring transformative therapies to patients worldwide.

Closing date for applications: 06 July 2026

Benefits & Rewards

The pay range for this position at commencement of employment is expected to be between $248,500 and $461,500 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

Salary Range
$248,500.00 - $461,500.00

Skills Desired
Cross-Functional Teamwork, Leadership, Medical Strategy (Inactive), Multicultural Leadership, Process Safety Management, Regulatory Compliance, Safety Science, Strategy (Inactive)

About Alcon

Alcon is a global medical company specializing in eye care products and services. The company's products include surgical equipment, contact lenses, and eye drops. Alcon was founded in 1945 and is headquartered in Baar, Switzerland. The company operates in over 70 countries and has over 20,000 employees. In 2019, Alcon became an independent publicly traded company after being spun off from Novartis.
Learn more about Alcon
Size
24,389 employees
Market Cap
$33.3 billion
Industry
Founded
1945
NASDAQ

Similar Jobs

More Jobs at Alcon

More Pharmaceuticals & Biotech Jobs

Find similar Sr. Global Program Safety Team Lead - Oncology jobs: