pharmacovigilance scientist

ProPharma

<div>
 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality &amp; compliance, pharmacovigilance, medical information, and R&amp;D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners&rsquo; most high-profile drug and device programs.
 
 
 
 Job Summary
 
 
 
 The Pharmacovigilance (PV) Scientist supports the activities in the Benefit Risk group by ensuring that day-to-day operational activities are completed. The PV Safety Scientist is expected to be professional and diligent and liaise with the director and management group members within the team on any issues, as well as coordinate the work with the senior PV Scientists. The PV Safety Scientist is also expected to lead by example and ensures quality standards are upheld within the company.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Authoring of Aggregate reports (PSURs/PBRERs, PADERs/Annual Reports/ ACO/ DSUR) for submission to local and other Health Authorities.
 </li>
 <li>
 Authoring of Risk Management Plans (RMPs) as a part of regular Pharmacovigilance activities.
 </li>
 <li>
 Authoring of Signal Management Reports.
 </li>
 <li>
 Performing literature search and validity check for the aggregate reports.
 </li>
 <li>
 Reconciliation of relevant process trackers.
 </li>
 <li>
 Extraction and validation of data (RSI, Sales, previous reports, RMP, signals).
 </li>
 <li>
 Generation of Line Listings (LL) from safety database
 </li>
 <li>
 </li>
 <li>
 Providing reliable support for high priority Ad-hoc activities.
 
 
 </li>
 </ul>
 
 Necessary Skills And Abilities.
 
 
 
 <ul>
 <li>
 Analytical and problem-solving skills.
 </li>
 <li>
 Sound organizational skills
 </li>
 <li>
 Able to work within a team in an open and professional manner
 </li>
 <li>
 Excellent attention to detail and focus on quality
 </li>
 <li>
 Understanding of ICH-GCP, FDA, EMA and other relevant Global regulations related to PV
 </li>
 <li>
 Demonstrable ability to analyze and quantify large volumes of data in a concise and scientific manner, in keeping with regulatory deadlines.
 </li>
 <li>
 Awareness of global culture and willingness to work in a matrix environment
 </li>
 <li>
 Knowledge in other pharmacovigilance processes, ability to author/update SOPs or WIs, to identify and author deviations/CAPAs."
 </li>
 <li>
 Ensuring that deliverables to the clients comply with the relevant regulatory requirements and are sent to the client within agreed timelines.
 </li>
 <li>
 Capability to make concise, accurate and relevant synopses of medical text and data, and the ability to write unambiguous medical text
 </li>
 <li>
 Computer proficiency, IT skills, expertise and an ability to work with web based applications, and familiarity with the Windows Operating system and the MS Office suite (Word/Excel/Power Point)
 
 
 </li>
 </ul>
 Educational requirements
 
 
 <ul>
 <li>
 Bachelor/master&rsquo;s degree in pharmacy, Nursing, Life Science, or other health-related field, or equivalent qualification/work experience
 
 
 </li>
 </ul>
 
 Experience Requirements
 
 
 
 <ul>
 <li>
 2+ years&rsquo; experience in Pharmacovigilance with a focus on medical writing and/or literature search and/or signal detection
 </li>
 <li>
 Experiences in contributing to the compilation of metrics and participating in discussions about quality internally and with Clients
 </li>
 <li>
 Experience in literature screening activities and/or experiences in authoring and reviewing aggregate reports
 
 
 </li>
 </ul>
 We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
 
 
 ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
</div>

Pharmacovigilance Safety Scientist

Alpha-9 Oncology

<div>
 
 Your Impact
 
 
 
 Alpha-9 Oncology is seeking a Pharmacovigilance Scientist to support drug safety activities across our early-phase clinical programs. You will establish foundational processes and operations, oversee vendor-delivered case processing, and ensure compliance with global safety requirements. This hands-on role offers the opportunity to shape how PV operations are built and scaled in a growing clinical stage radiopharmaceutical company.
 
 
 
 How You'll Contribute
 
 
 
 <ul>
 <li>
 Serve as the internal lead for PV operations, partnering with CROs, internal and external medical safety experts to ensure timely and accurate case processing, reconciliation, and safety reporting.
 </li>
 <li>
 Manage the collection, review, and quality oversight of safety data from clinical trials, including expedited and periodic reporting to regulatory authorities.
 </li>
 <li>
 Conduct and document literature surveillance and aggregate safety data review to identify potential safety signals.
 </li>
 <li>
 Support development of safety sections of regulatory documents (e.g., investigator brochures, DSURs, clinical study reports).
 </li>
 <li>
 Maintain inspection-ready safety documentation and contribute to the authoring and updating of PV SOPs and work instructions.
 </li>
 <li>
 Collaborate with Clinical Operations, Regulatory Affairs, and Quality to align safety processes with overall program execution.
 </li>
 <li>
 Contribute to vendor oversight, including review of safety deliverables, metrics, and compliance reports.
 
 
 </li>
 </ul>
 
 The Skills You Bring
 
 
 
 <ul>
 <li>
 Advanced degree (PharmD, RN, Ph.D., MPH, or MS) in a scientific or health-related field.
 </li>
 <li>
 3+ years of pharmacovigilance experience in biotech, pharma, or CRO settings.
 </li>
 <li>
 Hands-on experience with case processing, safety data reconciliation, and aggregate report contributions.
 </li>
 <li>
 Knowledge of global PV requirements (ICH, FDA, EMA, CIOMS, TGA) with practical application in early-phase clinical studies.
 </li>
 <li>
 Strong analytical and written communications kills, with the ability to synthesize and interpret safety data.
 </li>
 <li>
 Experience with CROs and vendors in a lean, fast-paced, early-stage biotech environment.
 </li>
 <li>
 Familiarity with safety databases and Microsoft Office tools.
 
 
 </li>
 </ul>
 
 What's In It For You
 
 
 
 At Alpha-9 Oncology, we offer a competitive and comprehensive benefits package designed to support all employees. Our benefits include a competitive salary, bonus, equity, 20 vacation days, 5 sick days, a technology allowance, and commuter reimbursement. We also provide generous retirement savings plans with employer matching, extended health benefits, and paid holidays, tailored to local standards in each region. While specific offerings may vary by location, our commitment to fostering a supportive and rewarding work environment is consistent across the company.
 
 
 
 Company Summary
 
 
 
 Alpha-9 Oncology is a clinical-stage biotechnology company pioneering radiopharmaceutical innovation for solid tumors. Our proprietary scaffolds, composed of optimized binders, linkers, chelators, and radioisotopes, enable targeted radiation delivery to cancer cells, minimizing harm to surrounding healthy tissue. Focusing on innovative targeting moieties, we develop molecules tailored for precise tumor targeting.
 
 
 Our comprehensive platform integrates imaging and therapeutic studies to ensure effective radiation delivery and improved patient outcomes. With a robust pipeline entering clinical trials and strong support from leading healthcare investors, Alpha-9 is positioned for rapid growth and advancement in cancer therapy.
 
 
 
 More About Alpha-9 Oncology
 
 
 
 Alpha-9 Oncology is committed to fostering a diverse and inclusive workplace and is proud to be an Equal Opportunity Employer. We provide employment opportunities to all qualified applicants without regard to race, ethnicity, religion, age, sex, gender identity or expression, sexual orientation, disability, marital status, family status, national origin, or any other characteristic protected by applicable federal, provincial, or local laws where we operate.
 
 
 We are dedicated to providing reasonable accommodations to qualified applicants and employees to ensure that everyone can perform their essential job functions in an inclusive environment. For inquiries regarding accommodations in the hiring process or for current employees, please contact a member from our Talent Acquisition team.
</div>

Scientist, Pharmacovigilance

<div>Site Name: UAE - Dubai 
Posted Date: Nov 18 2025 
Position Summary
We are inviting UAE Nationals to join our Pharmacovigilance team in the UAE as a Pharmacovigilance Associate. In this role you will collect, assess and report safety information in accordance with local and global regulatory requirements. You will collaborate with safety scientists, medical experts and cross-functional partners to support timely case management, signal detection and regulatory reporting. We are seeking team members who value accuracy, clear communication, ethical conduct and continuous learning.
Key Responsibilities<ul><li>
Receive, document and triage safety reports from healthcare professionals, patients and internal colleagues, ensuring confidentiality of personal data at all times.</li><li>
Perform initial case assessment and follow-up to obtain complete and accurate information for case evaluation.</li><li>
Accurately enter case data into pharmacovigilance databases and maintain data quality and completeness.</li><li>
Prepare and submit safety reports to health authorities and internal stakeholders according to local and company reporting timelines and procedures.</li><li>
Support routine safety reporting, expedited reporting and signal detection activities in line with company and regulatory requirements.</li><li>
Collaborate with cross&#8209;functional teams (medical affairs, clinical, regulatory, legal, commercial) to resolve safety queries and support compliance activities.</li><li>
Adhere to GSK policies on patient privacy, data protection, pharmacovigilance SOPs and ethics.</li></ul>
Basic Qualifications<ul><li>
UAE National with family book.</li><li>
Bachelor&rsquo;s degree in pharmacy, life sciences, nursing, medicine or a related discipline.</li><li>
Previous exposure to pharmacovigilance, drug safety, or a clinical/healthcare environment.</li><li>
High attention to detail, accuracy in data entry and good organisational skills.</li><li>
Strong written and verbal communication skills in English; Arabic language skills are an advantage.</li><li>
Proficiency in Microsoft Office applications.</li></ul>
Preferred Qualifications<ul><li>
Experience with safety databases, case management systems or pharmacovigilance tools.</li><li>
Knowledge of UAE pharmacovigilance regulations and local reporting timelines.</li><li>
Formal pharmacovigilance/drug safety training or certification.</li><li>
Able to manage multiple priorities and meet regulatory deadlines.</li><li>
Experience engaging with health authorities, healthcare professionals or working in multinational teams.</li></ul>
Additional Information: 
This role is based on-site in Dubai, United Arab Emirates.
Application Process: 
If you&rsquo;re ready to grow your skills, make a positive impact, and contribute to GSK&rsquo;s mission, apply today!
GSK is an equal opportunity employer and values diversity, equity, and inclusion. We welcome applications from UAE Nationals who are passionate about improving lives and ensuring compliance with local regulations.
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Pharmacovigilance Associate - UAE National

Acino

<div>Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide. 
This position is based in Cairo, Egypt and will report directly to the Pharmacovigilance Head META. The role will be responsible for monitoring, assessing, and reporting the safety of pharmaceutical products, ensuring compliance with global regulatory standards. 


Your Responsibilities will be: 
Safety Data Exchange Agreements (SDEAs)
<ul>
<li>Draft, negotiate, and maintain SDEAs with business partners in META region in compliance with corporate and regulatory requirements.</li>
<li>Ensure timely execution and periodic review of SDEAs, including reconciliation of safety responsibilities and timelines in coordination with GPV.</li>
<li>Track SDEA obligations and ensure alignment with internal SOPs and global PV standards.</li>
<li>Coordinate with legal, regulatory, and compliance teams to ensure contract integrity and audit readiness.</li></ul> 


Business Partner (BP) Communication
<ul>
<li>Act as the primary PV liaison for regional business partners, distributors, and license holders.</li>
<li>Ensure timely exchange of safety data and compliance with agreed pharmacovigilance obligations.</li>
<li>Provide PV Onboarding/Refreshing training to BPs in alignment with global procedures.</li>
<li>Monitor BP compliance metrics and escalate deviations or risks as needed.</li></ul> 


Management of Internal CAPAs and deviations
<ul>
<li>Managing internal CAPAs and deviations in TrackWise, documenting quality events, assigning corrective actions, tracking progress, and ensuring compliance through automated workflows and audit-ready records.</li></ul> 


Global PSMF Maintenance
<ul><li>Ensure Global PSMF remains accurate, up-to-date, and compliant with regulatory requirements across all applicable regions.</li>
<li>Maintain the regional annexes of the Global Pharmacovigilance System Master File (PSMF)</li></ul> 


Assigned tasks from GPV responsibilities
<ul>
<li>Conduct regular screening of scientific and medical literature to identify potential adverse events and ensure compliance with global pharmacovigilance requirements</li>
<li>Prepare and review periodic safety update reports (PSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs), and other aggregate safety reports to summarize the benefit-risk profile of medicinal products.</li>
<li>Develop and maintain risk management plans (RMPs) to proactively identify, assess, and mitigate safety risks associated with pharmaceutical products.</li>
<li>Perform signal detection and evaluation activities to identify new safety concerns and trends from various data sources</li>
<li>Performs other tasks under direction of Director PV Operations if requested.</li></ul> 


SOPs management
<ul>
<li>Oversee the development, implementation, and periodic review of pharmacovigilance Standard Operating Procedures (SOPs) to ensure regulatory compliance, operational consistency, and alignment with global quality standards.</li></ul> 


Your Profile: 
<ul>
<li>
A university degree in Pharmacy, Medicine, Life Sciences, or related field.</li>
<li>Minimum 5-8 years&rsquo; experience in pharmacovigilance, with direct experience managing SDEAs and partner communications.</li>
<li>Excellent user of MS Office applications (Word, Excel, PowerPoint, Outlook).</li>
<li>Ability to learn about new technologies, strategies and policies, with high level of compliance with policies. Experience with electronic systems and databases.</li>
<li>Fluent in English, both in oral and in writing.</li>
<li>Full understanding of legal/compliance environment and requirements.</li></ul> 


This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!</div>

Senior Pharmacovigilance (PV) Specialist META

Arrowhead Pharmaceuticals

<div>
 Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead&rsquo;s RNAi-based therapeutics leverage this natural pathway of gene silencing.
 
 
 Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
 
 
 Arrowhead&rsquo;s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
 
 
 
 The Position
 
 
 
 The Senior Medical Scientist, Drug Safety will provide operational and scientific support in managing the development, implementation and oversight of Arrowhead investigational products with engaging in, but not limited to: support safety governance and surveillance procedures including safety reporting processes, advanced safety analytics, expedited and periodic aggregate reports ensuring compliance with internal standard operating procedures, FDA and global safety reporting requirements. They will conduct trend recognition, signal detection, and assist in overseeing relationships with vendors and business partners to ensure the highest quality of safety data is collected, reviewed and analyzed which fulfill all safety reporting requirements are met in the required timelines.
 
 
 This role will collaborate with Drug Safety Operations, Safety Scientists, medical monitors, clinical operations, QA, Data Management and regulatory colleagues in the set-up of and support of clinical development programs and/or post-marketed products to ensure safety oversight.
 
 
 This role is based fulltime onsite 5 days a week in San Diego, CA.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Safety Science Responsibilities
 </li>
 <ul>
 <li>
 Review potential safety observations, safety signals and contribute to the Safety Review Committee and Safety Governance process through the preparation and presentation of safety data; prepare and assess safety data for ongoing periodic, aggregate safety data reviews, and provide recommendations for review and approval by the Executive Safety Committee
 </li>
 <li>
 Prepare periodic aggregate safety reports including PSUR, DSUR, FDA IND Annual Report etc.
 </li>
 <li>
 Performs routine signal detection, identifies and evaluate safety signals
 </li>
 <li>
 Continually stay up to date on relevant regulations associated with the above activities
 </li>
 <li>
 Develop and update of Safety Surveillance Plans for assigned products
 </li>
 <li>
 Supports the preparation and maintenance of safety sections of the Clinical Protocols, Clinical Study Reports, Company Core Data Sheet, Investigators Brochure and Risk Management Plan
 </li>
 <li>
 Assist in quality assurance activities, including deviation reports
 </li>
 <li>
 Monitor SAE reconciliation with the Arrowhead PV vendor and study CRO to ensure effective reconciliation process
 </li>
 <li>
 Assist with preparation for regulatory inspections including a compiling of material relating to safety/pharmacovigilance reports and activities
 </li>
 <li>
 Support activities associated with launching a filing for the BLA/NDA or global marketing
 </li>
 </ul>
 <li>
 Medical Review Responsibilities
 </li>
 <ul>
 <li>
 Perform Medical Review on SAE/SUSAR if applicable
 </li>
 <li>
 Conduct active case follow-up, including written and verbal follow-up with clinical operations, clinical investigators and sites if applicable
 
 </li>
 </ul>
 </ul>
 
 Requirements:
 
 
 
 <ul>
 <li>
 Medical Degree: MD/DO
 </li>
 <li>
 8 years in the pharmaceutical industry or CRO
 </li>
 <li>
 5 years in drug safety operations, pharmacovigilance, and/or a similar combination of education and experience
 </li>
 <li>
 Experience in Signal Detection and Safety Data Analytics
 </li>
 <li>
 Strong safety science experience to utilize data analysis and visualization platforms and tools by applying advanced scientific algorithms and methods and translating the strategic vision of safety science into risk mitigation strategies and data visualization insights
 </li>
 <li>
 Strong working knowledge of FDA and international adverse event reporting regulations {ICH, EMA GPV, GCP etc.) and the ability to interpret and apply applicable regulations
 </li>
 <li>
 Strong working knowledge of ARGUS case management and processing; experience in using ARGUS or other safety databases; experience with MedDRA/WHODrug for coding AEs, medical history, and concomitant medications
 </li>
 <li>
 Experience with preparation with aggregate reports, preferably for investigational drugs (i.e., DSURs, IND Annual reports) or post-marketing products (i.e., PSUR/PBRER, PADERs)
 </li>
 <li>
 Strong interpersonal skills with the ability to professionally interact with cross functional team members
 
 
 </li>
 </ul>
 California pay range
 
 
 $195,000&mdash;$220,000 USD
 
 
 Arrowhead provides competitive salaries and an excellent benefit package.
 
 
 All applicants must have authorization to work in the US for a company.
 
 
 California Applicant Privacy Policy
</div>

Senior Medical Scientist, Drug Safety

IQVIA

<div>Associate Business Analyst
 
As an Associate Business Analyst within the IQVIA IVP Product Team, you will play a key role in supporting business analysis activities for our pharmacovigilance and safety products. You will assist in understanding business requirements, documenting system workflows, and collaborating with cross-functional teams to ensure the delivery of high-quality, compliant, and user-focused solutions for global life sciences clients.
 
 
This role is ideal for recent graduates or professionals with up to 1 year of experience who are passionate about healthcare technology, data-driven decision-making, and digital transformation in pharmacovigilance.
Role Responsibilities Work closely with Product Managers and Delivery Teams to gather, analyze, and document business and functional requirements.
 
 
Participate in requirement discussions, user story creation, and backlog grooming sessions for IVP products.
 
 
Translate business needs into clear and concise documentation such as Business Requirement Documents (BRD), User Stories, and Use Cases.
 
 
Assist in validating business workflows, performing data checks, and supporting testing activities to ensure alignment with user expectations.
 
 
Contribute to creating and maintaining documentation in Confluence and tracking tasks in Jira.
 
 
Support UAT (User Acceptance Testing) and coordinate with QA teams to ensure test coverage for business scenarios.
 
 
Participate in continuous improvement initiatives to enhance product usability and process efficiency.
 
 
Gain domain knowledge in pharmacovigilance, safety case management, and life sciences data workflows.
 
 
Support communication and coordination between business stakeholders, technical teams, and project managers.
 
 
Ensure adherence to defined processes, quality standards, and documentation best practices.
Minimum eligibility criteria Bachelor&rsquo;s or Master degree in Life Sciences, Pharmacy, Computer Science, Engineering, or related fields.
 
 
0&ndash;1 year of professional experience in Business Analysis or related roles within healthcare, life sciences, or pharmacovigilance domains.
 
 
Strong analytical and problem-solving skills with a keen attention to detail.
 
 
Excellent verbal and written communication skills.
 
 
Ability to work collaboratively in a fast-paced, global team environment.
Technology exposure Familiarity with Salesforce CRM, Jira, and Confluence tools.
Additional / nice-to-have criteria Understanding of software development lifecycle (SDLC) and agile methodologies.
 
 
Exposure to data-driven healthcare or pharmacovigilance systems.
 
 
Awareness of regulatory compliance standards such as GxP or 21 CFR Part 11.
 
 
Basic understanding of reporting, dashboards, or data visualization tools.
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</div>

Associate Business Analyst

Exeltis Turkey

<div>
 
 
 Medical Manager
 
 
 
 
 
 
 We are looking for a Medical Manager to be assigned to our Head Office at Exeltis Turkey.
 
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Medical Doctor (MD) degree,
 </li>
 <li>
 Excellent command of written and spoken English,
 </li>
 <li>
 Proficient in MS Office applications and effective presentation techniques,
 </li>
 <li>
 Strong sense of responsibility with analytical and strategic thinking skills,
 </li>
 <li>
 Holder of a valid B-class driving license and actively driving,
 </li>
 <li>
 No restrictions on travel.
 </li>
 <li>
 Experience in Respiratory Field will be preferred
 </li>
 </ul>
 
 
 
 
 
 Job Description
 
 
 <ul>
 <li>
 Providing continuous medical update and support for existing products,
 </li>
 <li>
 Represent the company at Scientific Congresses, trainings, and medical meetings,
 </li>
 <li>
 Provide medical support to Marketing and Sales teams during scientific presentations,
 </li>
 <li>
 Contribute medical insights to product strategies,
 </li>
 <li>
 Conduct meetings with key opinion leaders (KOLs) and Health Authorities regarding assigned products,
 </li>
 <li>
 Plan, initiate, and monitor clinical research activities,
 </li>
 <li>
 Oversee pharmacovigilance operations and ensure the pharmacovigilance system remains compliant with current regulatory requirements
 </li>
 </ul>
 
 
</div>

Medical Manager

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