3 Development specialist Jobs and Work in Bloemfontein Free State

Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2)
IQVIA —Bloemfontein, Free State
- R1 534 119 a year
- Full-time
HEAD OF ACADEMICS
Advtech —Bloemfontein, Free State
7h
Associate Professor/Professor: Childhood Education
University of the Free State —Bloemfontein, Free State
4d

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HEAD OF ACADEMICS
Advtech —Bloemfontein, Free State
3 - 5 years experience in an academic administration position in a decentralized setting. 3 - 5 years experience in a general management position.
7h

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Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2)

IQVIA -
Bloemfontein, Free State

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Job Details

Full-time
R1 534 119 a year

Full Job Description

Bloemfontein, South Africa | Full time | Hybrid | R1534119

Duties/Responsibilities:

Act as signal detection and literature lead, or back-up lead to contribute to the conduct of ongoing literature safety surveillance for marketed and investigational products, evaluating events of special interests as well as aggregate data review
Author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs and ACOs.
Author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
Can serve as principal owner (molecule lead) for the molecule and have responsibility for completion of the deliverable and in compliance with all applicable Key performance indicators (KPI); Set-up and update products' signaling strategies, as approved by the customer’s Safety Strategy Lead. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks, as approved by the customer’s Safety Strategy Lead. Responsible for full documentation and tracking of signals.
Ensuring the completion of molecule deliverables on time and liaise with portfolio clinical science scientists, service provider process leads and cross-functional stakeholders.
Distribution of molecule work within team consisting of molecule scientists, when necessary, coordinating support across molecules and disease areas when there are peaks and troughs in workload.
End-to-end molecule work oversight and responsibility (i.e., ensuring consistent tracking of signals from detection to assessment to inclusion in aggregate reports).
Ensuring an in-depth knowledge of the molecule and disease area within the service provider molecule team.
Oversight and responsibility of quality-of molecule deliverables to the customer’s molecule team, with “hands-on” involvement, i.e., involved in authoring DSR conclusion, participating in SD/Lit meetings between service provider and customers.
Responsible for resolution of issues on molecule deliverables (if necessary, in collaboration with service provider process lead).
Participate in internal and external audits and inspections, as required.
Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion to maintain compliance and documented
Conduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members.

Qualifications:

Life science graduate/post-graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
4-6 years of relevant experience in Pharmacovigilance including hands-on experience of drug safety, aggregate reports, signal detection/signal management preferred
Excellent communication (written and verbal) skills
Team working
English – fluent (spoken, written)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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development specialist jobs in bloemfontein free state

Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2)

HEAD OF ACADEMICS

Associate Professor/Professor: Childhood Education

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I want to receive the latest job alert for development specialist in bloemfontein free state

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