Global Aviation Security Strategist—Remote

Placements24; Klerksdorp; Remote; ZAR 450,000 - 800,000; Full time

Benefits offered by this job

Health benefits

Job summary

Thermo Fisher Scientific is seeking a Pharmacovigilance Scientist to coordinate signal detection and safety activities across products. You will mentor junior staff, help develop processes and tools, and may lead smaller FSP-type engagements with clients and audits.

The role emphasizes applying PV expertise to ensure safety compliance and timely regulatory reporting, with opportunities for career growth and professional development within a global team.

Qualifications

• Bachelor's degree required in a related field.
• Experience in pharmacovigilance and signal detection.
• Knowledge of regulatory requirements across major markets.

Responsibilities

• Plan, coordinate and deliver signal detection and product safety tasks.
• Mentor junior colleagues and contribute to process/tool development.
• Lead small projects and participate in client communications and audits.

Skills

Pharmacovigilance

Signal detection

Regulatory compliance

Client advisory

Mentoring

Education

Bachelor's degree

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Our detailed, goal-oriented team members manage the safety profile of new drugs in clinical trials, oversee case-processing activities through all phases of development and perform regulatory reporting and medical monitoring tasks.
We hire the best, develop ourselves and each other, and recognise the power of being one team. We offer continued career advancement opportunities, award-winning training and benefits focused on the health and wellbeing of our employees.
A Day in the Life:
Responsible for the planning, coordination and delivery of signal detection and product safety scientist activities, with a focus on tasks which are low to high in complexity or which concern low to high complexity products. Additionally supports mentoring of more junior colleagues, development of processes/tools/systems, and may serve as lead on smaller FSP-type projects.

Essential Functions

• Serves as a creator/contributor for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products.
• Serves as a creator/contributor for signal detection and product safety scientist tasks which are ultra-high in complexity, or which concern ultra-high complexity products, under supervision by a more experienced team member.
• Conducts quality review for signal detection and product safety scientist tasks which are low to high in complexity, or which concern low to high complexity products.
• Advises clients on safety related issues under supervision by a more experienced team member.
• Leads small FSP projects.
• Supports training and mentoring of junior colleagues.
• Contributes to development of processes, tools and systems.
• Participates in bid defence and proposal development activities.
• Works within multiple company and client systems. Interacts with project team members and clients.
• Ensures that tasks are conducted in accordance with company policies and procedures, contractual agreements, and applicable regulations.
• Participates in departmental initiatives; Serves as a subject matter expert in designated area.
• Responsible for routine project implementation and coordination for assigned projects, including leading kick-off meetings, coordination of communications and data requests, participation in client meetings, audits and inspections, and review of metrics and budgets.
• Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
• Having wide-ranging experience, uses professional concepts and company objectives to resolve complex issues in creative and effective ways.
• Determines methods and procedures on new assignments and may coordinate activities of other personnel (i.e., Team Lead). Exercises' judgment in selecting methods, techniques and evaluation criteria for obtaining results.
• Frequent contacts with internal personnel and outside customer representatives.

Keys to Success

Education and Experience:

• Bachelor's degree
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

Knowledge, Skills and Abilities

• Expertise in pharmacovigilance requirements relating to marketed products and clinical trials across all major markets
• Excellent attention to