Pharmacy Jobs

Role & Responsibilities • Promote company’s therapy-focused pharmaceutical products to specialist doctors • Develop strong scientific engagement and long-term professional relationships with consultants • Conduct effective product detailing with strong clinical knowledge • Organize CMEs, RTMs, and scientific promotional activities • Achieve therapy-wise prescription generation and sales targets • Monitor competitor brands and market trends in the therapy segment • Ensure product availability at hospitals and key pharmacies • Maintain daily call reports, doctor data, and sales records Qualification • B.Sc (Biology) / B.Pharm Experience • Minimum 1–2 years of pharmaceutical field sales experience • Experience in specialty/therapy segment preferred Skills • Strong therapy and product knowledge • Scientific communication ability • Relationship building with specialist doctors • Target-oriented approach • Good presentation and interpersonal skills About Company Unifaith Biotech Private Limited is a growing pharmaceutical company focused on delivering quality healthcare solutions. The company emphasizes scientific promotion, strong doctor relationships, and expanding its presence in specialized therapy segments.

Roles & Responsibilities • Dispense prescribed medications accurately in compliance with MOH regulations. • Review prescriptions to ensure correct dosage, strength, and instructions. • Counsel patients on medication usage, dosage, storage, and possible side effects. • Maintain proper storage conditions and monitor medicine expiry dates. • Manage inventory, stock levels, and pharmacy records. • Ensure compliance with UAE pharmacy laws, safety standards, and SOPs. • Maintain cleanliness, organization, and professional standards within the pharmacy. Eligibility Criteria • MOH Qualified Pharmacist (mandatory). • Male candidates preferred. • Pashto (Pastun) language proficiency preferred. • Fresher or experienced candidates can apply. • Willingness to work in Ajman. Skills • Good communication and customer-handling skills. • Strong attention to detail and accuracy. • Ethical and professional approach to patient care. • Ability to work independently and responsibly. Application Details Only interested candidates are requested to share their CV at: 📧 zonepharmacyuae@gmail.com About the Company Zone Pharmacy is a community-focused pharmacy in Ajman, UAE, committed to providing safe, reliable, and patient-centric pharmaceutical services. The pharmacy emphasizes professional ethics, regulatory compliance, and high-quality healthcare support to meet the everyday needs of the community.

Roles & Responsibilities • Assist licensed pharmacists in dispensing medications accurately. • Support prescription review, labeling, and medicine preparation under supervision. • Counsel customers on basic medication usage, storage, and safety guidelines. • Maintain cleanliness, organization, and hygiene of the pharmacy area. • Assist in inventory management, stock checking, and expiry monitoring. • Ensure adherence to pharmacy SOPs, DHA/MOH guidelines, and ethical practices. • Support daily pharmacy operations and customer service activities. Qualification • Bachelor’s degree in Pharmacy (B.Pharm). Experience • Freshers or entry-level candidates are eligible to apply. Skills • Good communication and interpersonal skills. • Willingness to learn and adapt in a pharmacy environment. • Customer-focused attitude with attention to detail. • Ability to work effectively in a team setting. • Basic understanding of pharmaceutical products and practices. About the Company AxessMed Pharmacy is a trusted healthcare and pharmacy services provider in the UAE, dedicated to delivering high-quality pharmaceutical care and patient-centered services. The organization emphasizes professional development, regulatory compliance, and ethical practices while creating opportunities for young pharmacy graduates to build strong careers in a dynamic healthcare environment.

Roles & Responsibilities • Dispense prescribed medications accurately in compliance with UAE pharmacy regulations. • Review prescriptions to ensure safety, accuracy, and therapeutic appropriateness. • Counsel patients on medication usage, dosage, precautions, and possible side effects. • Ensure proper storage, labeling, and handling of medicines as per DHA/MOH guidelines. • Monitor inventory levels, manage stock, and remove expired or damaged medicines. • Maintain accurate documentation, records, and reports as required by authorities. • Adhere strictly to DHA/MOH regulations, SOPs, and ethical pharmacy practices. • Support smooth day-to-day pharmacy operations and collaborate with team members. Qualification • Bachelor’s degree in Pharmacy (B.Pharm). • Valid DHA or MOH eligibility/license (mandatory). Experience • Minimum 2 years of pharmacy experience in the UAE. Skills • Strong knowledge of medicines and UAE regulatory requirements. • Excellent communication and patient-counseling skills. • Ability to work independently and in a team environment. • Strong attention to detail and professional ethics. • Arabic proficiency is mandatory. Additional Requirements • Ready to work in any Emirate across the UAE. • Immediate joiners preferred. About the Company AxessMed Pharmacy is a growing healthcare and pharmacy services provider in the UAE, committed to delivering safe, reliable, and patient-focused pharmaceutical care. With a strong emphasis on regulatory compliance, professional ethics, and customer satisfaction, AxessMed Pharmacy aims to enhance community health by offering quality medicines, expert guidance, and trusted healthcare services across its network.

Elmed Life Sciences Pvt Ltd, a leading USFDA-registered pharmaceutical formulation unit specializing in probiotics and OSD manufacturing, is hiring experienced professionals for its Oral Solid Dosage (OSD) department in Cherlapally, Hyderabad.Date: Saturday, 6th December 2025 Time: 10:00 AM – 3:00 PM Venue: Plot No. 36, Phase V, IDA Cherlapally, Hyderabad, Telangana – 500051 Available Positions – OSD Department Only1. Production Assistant Manager (OSD)Qualification: B.Pharm / M.Pharm / B.Sc / M.ScExperience: 8–10 years in pharma manufacturingSalary Range: ₹7 – 9 LPAKey Skills Required:Hands-on experience in upstream & downstream fermentation (preferred)Complete production planning & execution in OSDRegulatory compliance (USFDA, WHO-GMP)Team handling & cross-functional coordinationDocumentation oversight, CAPA, change controlYield improvement & process optimizationWhy Join Elmed Life Sciences?USFDA & WHO-GMP certified facilityState-of-the-art probiotic & OSD manufacturingAttractive salary + statutory benefitsFast-track growth for performersJob stability with expanding export orders

Roles & Responsibilities: • Dispense prescribed medicines accurately as per doctor’s prescriptions. • Ensure proper storage, handling, and labeling of medicines in compliance with regulatory standards. • Maintain inventory levels, monitor expiry dates, and manage stock records. • Guide patients on correct dosage, usage instructions, and possible side effects. • Ensure compliance with pharmacy laws, State Pharmacy Council regulations, and SOPs. • Maintain accurate records of prescriptions, sales, and inventory. • Coordinate with suppliers for timely procurement of medicines. • Maintain cleanliness, organization, and safety within the pharmacy. Qualification: • Diploma in Pharmacy (D.Pharm) or Bachelor of Pharmacy (B.Pharm). • Registered Pharmacist with the State Pharmacy Council (mandatory). Experience: • Freshers and experienced candidates can apply. Skills: • Good knowledge of medicines and pharmaceutical practices. • Strong attention to detail and accuracy. • Good communication and customer-handling skills. • Knowledge of pharmacy software and billing systems (preferred). • Ability to work independently with a responsible and ethical approach. About the Organisation: Empera Meditech India Private Limited is a growing healthcare organization committed to delivering reliable pharmaceutical products and patient-focused services. The company emphasizes ethical practices, regulatory compliance, and quality healthcare delivery, providing professionals with a supportive environment to develop their skills and build a stable career in the pharmaceutical sector.

Roles & Responsibilities: • Compound and dispense medications as prescribed by physicians. • Monitor customers’ drug therapies, advise interventions, and inform about potential side effects. • Instruct customers on proper use and timing of prescribed medications. • Conduct health and wellness screenings. • Provide immunizations and basic medical services (blood pressure, temperature, blood sugar checks). • Maintain accurate customer records. • Ensure a safe, clean, and compliant pharmacy environment. • Complete operational pharmacy requirements, including verifying orders, maintaining controlled substance records, and removing expired/damaged drugs. • Adhere to legal and regulatory requirements governing pharmacy practice. • Perform other administrative tasks as needed. Qualification: • Bachelor’s degree in Pharmacy or Pharmacology. • Valid State Pharmacy Registration License (mandatory). Experience: • Minimum 1 year of work experience as a pharmacist. Skills: • Detailed understanding of dosages, chemical compounds, and pharmaceutical brands. • Proficient in Microsoft Office Suite and pharmacy software (e.g., MEDITECH, Mediware). • Excellent organizational, verbal, and written communication skills. • Ability to work independently and provide patient-centered care. About the Organisation:Indira IVF Hospital Pvt Ltd is committed to delivering high-quality pharmaceutical care and ensuring patient safety. With a focus on compliance, customer service, and professional development, the organisation provides pharmacists a structured environment to grow their skills, serve the community, and advance their careers.

Roles & Responsibilities: • Medication Dispensing: Review prescriptions, accurately compound, package, and label medicines. • Inventory Management: Maintain stock records, monitor inventory levels, and remove expired/damaged products. • Regulatory Compliance: Ensure adherence to pharmacy laws, regulations, and State Pharmacy Council standards. • Prescription Verification: Check prescriptions for accuracy and identify therapeutic incompatibilities. • Operational Support: Oversee pharmacy technicians and ensure smooth daily operations. Qualification: • D.Pharm or B.Pharm from a recognized institution. • Valid State Pharmacy Registration License (mandatory, including for freshers). Experience: • Freshers preferred – great opportunity to start a pharmacy career. Skills: • Strong attention to detail and organizational ability. • Excellent communication and interpersonal skills. • Ability to work independently and collaboratively in a team. • Customer-oriented mindset. • Sound knowledge of pharmaceutical sciences, dosages, and prescription verification. • Familiarity with pharmacy information systems is an advantage. About the Organisation:Eminent India Pvt ltd is committed to providing high-quality healthcare services and patient care. With a focus on professional pharmacy practices, regulatory compliance, and customer satisfaction, the organisation offers a supportive environment for freshers to learn, grow, and build a successful career in pharmacy.

Roles & Responsibilities: • Dispense medicines accurately as per prescriptions and ensure patient safety. • Provide counseling and advice on proper medication use and potential side effects. • Maintain pharmacy records, stock, and inventory in compliance with regulatory standards. • Ensure adherence to Good Pharmacy Practices (GPP) and legal requirements. • Assist in day-to-day operations of the pharmacy, including billing, stock management, and customer service. • Maintain hygiene, cleanliness, and professional standards in the pharmacy environment. Qualification: • B.Pharm or D.Pharm required.Skills: • Strong knowledge of pharmacology, drug interactions, and dosage guidelines. • Good communication and counseling skills for patient interactions. • Attention to detail and accuracy in dispensing medicines. • Organizational and record-keeping skills. • Ability to manage inventory and handle pharmacy software systems. • Customer service orientation and professional ethics. About the Organisation: Apollo Pharmacy is one of India’s largest retail pharmacy chains, dedicated to providing high-quality healthcare products and services. With a vast network of stores nationwide, Apollo Pharmacy focuses on patient safety, professional pharmacy practices, and accessible healthcare solutions, fostering a culture of trust, innovation, and excellence in pharmaceutical retail.

Roles & Responsibilities: • Dispense medicines accurately as per prescriptions and ensure patient safety. • Provide counseling and advice on proper medication use and potential side effects. • Maintain pharmacy records, stock, and inventory in compliance with regulatory standards. • Ensure adherence to Good Pharmacy Practices (GPP) and legal requirements. • Assist in day-to-day operations of the pharmacy, including billing, stock management, and customer service. • Maintain hygiene, cleanliness, and professional standards in the pharmacy environment. Qualification: • B.Pharm or D.Pharm required. • Valid Tamil Nadu Pharmacist License / PCI Registration required. Skills: • Knowledge of pharmaceuticals, dosage forms, and patient counseling. • Strong communication and customer service skills. • Attention to detail and accuracy in dispensing and record-keeping. About the Organisation: Apollo Pharmacy is one of India’s largest retail pharmacy chains, committed to providing high-quality healthcare products and services. With a wide network of stores across the country, Apollo Pharmacy focuses on patient safety, professional pharmacy practices, and accessible healthcare solutions, while fostering a culture of trust, innovation, and excellence in the pharmaceutical retail sector.

Roles & Responsibilities: • Develop and implement sales strategies for assigned territory to achieve monthly, quarterly, and annual targets. • Promote company products ethically through science-based discussions with doctors, chemists, and other stakeholders. • Organize CMEs, retail meets, market blitzes, and other promotional activities as per division strategy. • Plan and execute merchandising, sampling, and brand visibility activities across clinics and trade. • Facilitate new product launches by identifying and targeting customers, ensuring proper engagement, and providing feedback. • Maintain and update customer and distributor databases; ensure 100% doctor coverage and regular customer interactions. • Monitor prescriptions for Abbott and competitor brands; collect market intelligence and retailer-level inventory data. • Manage distributor network including appointment, credit assessment, stock & sales statement tracking, and claim settlement. • Lead, mentor, and set example for junior team members in adherence to Abbott Code of Business Conduct, FCPA, and pharmacovigilance. • Ensure compliance with company financial, administrative, statutory, and regulatory systems. • Promote Abbott’s values—Pioneering, Achieving, Caring, Enduring—and ensure high-level customer service. • Participate in strategy meetings, workshops, training programs, and other company initiatives to drive performance and brand image. • Adhere to EHS policies, complete required trainings, wear safety gear, report incidents, and contribute to safety improvements. Qualification: • Graduate degree in Life Sciences, Pharmacy, or relevant field. Experience: • Relevant experience in pharmaceutical sales, brand management, or territory management preferred. Skills: • Strong communication, negotiation, and customer relationship management. • Strategic thinking and ability to execute business plans effectively. • Leadership and team mentoring capabilities. • Analytical skills for market intelligence, sales monitoring, and decision-making. • Knowledge of compliance, pharmacovigilance, and ethical promotional practices. About the Organisation: Abbott is a global healthcare company committed to improving lives through innovative medicines, diagnostics, and medical devices. The company emphasizes ethical practices, patient safety, and professional development while fostering a culture of care, innovation, and excellence.

Roles & Responsibilities: • Develop global regulatory project plans for moderate-to-high complexity submissions (CTA/IND, MAA/NDA/BLA, HA meetings/Scientific Advice). • Track regulatory deliverables, ensuring timely submission and life cycle management of products. • Collaborate with Global Regulatory Lead, Regulatory Affairs Manager, and Submission Manager to execute submissions. • Orchestrate Submission Task Force activities, manage risks, interdependencies, and resolve issues impacting timelines. • Set up hypercare for critical submissions to Health Authorities. • Consolidate budget planning and track actuals for regulatory projects; coordinate with project controllers and global project management. • Support operational aspects of in-licensing/out-licensing deals, including asset transfer planning and internal activity initiation. • Improve project management tools, templates, and ensure compliance with Health Authority requirements. • Maintain strong collaboration across cross-functional teams and matrix organization stakeholders. • Ensure documentation and dossier readiness, including CPPs, GMP Certificates, MLs, AtOs, AFs, CLs, PoAs, and legalization frameworks. • Manage regulatory affairs knowledge for post-approval changes, dossier types, and main global procedures. Qualification: • Degree in Life Sciences, Medicine, Pharmacy, PharmD, or related discipline (minimum MSc or equivalent; PhD preferred). • Advanced training in portfolio and project management preferred. Experience: • 8–14 years of work experience in pharmaceutical, regulatory authority, or R&D environments. • Minimum 6–8 years in regulatory affairs or regulatory project management. • Hands-on experience with global regulatory submissions and life cycle management. • Contributor-level experience with RIM and EDMS RA applications. Skills: • Excellent written and spoken English communication. • Strong project management, organizational, and result-oriented skills. • Ability to influence teams, work collaboratively in a matrix organization, and take ownership of deliverables. • Strong customer orientation, problem-solving, and strategic thinking. • Knowledge of EU & international regulatory requirements and frameworks. About the Organisation: A leading global pharmaceutical and life sciences company focused on innovative solutions for healthcare, life sciences, and electronics. The organization fosters a culture of curiosity, inclusion, and collaboration, emphasizing scientific excellence, regulatory compliance, and patient-centric innovation. Employees are encouraged to take ownership, innovate, and contribute to impactful global health outcomes.

Roles & Responsibilities: • Lead end-to-end dose surveillance activities across multiple clinical trials from start-up to close-out. • Perform routine and ad-hoc dose reviews, identify discrepancies, and coordinate follow-ups with sites and medical partners. • Document dose-related operational risks in SPOT/COSMOS, ensuring inspection-ready records. • Provide data-driven insights to trial teams, Clinical Monitoring Managers (CMMs), Medical Advisors, and functional stakeholders. • Ensure audit and inspection readiness, adhering to ICH-GCP, SOPs, and regulatory expectations. • Collaborate with Trial Managers on dosing and retention issues, strengthening relationships with site staff and internal partners. • Coach site staff to improve dose compliance and documentation quality. • Contribute to departmental training, knowledge sharing, and continuous improvement of surveillance methodologies. • Support global cross-functional improvement projects and drive innovation in dose surveillance processes. Qualification: • Graduate degree in Life Sciences (M-Pharma, PharmD, BDS/MDS, Pharmacy, MSc Nursing) with strong understanding of clinical trial conduct and ICH-GCP. Experience: • Minimum 4 years in clinical trials within pharmaceutical, biotech, CRO, or hospital settings. • Strong working knowledge of trial data, systems, and global clinical operations. • Experience collaborating with diverse global stakeholders. Skills: • Excellent communication, relationship-building, and stakeholder management skills. • Strong analytical mindset and familiarity with clinical IT systems. • Ability to independently solve complex issues in evolving environments. • High motivation, ownership, and continuous improvement mindset. • Ability to coach, influence, and guide site and internal staff effectively. About the Organisation: Novo Nordisk is a global biopharmaceutical company dedicated to defeating serious chronic diseases and improving long-term health outcomes. The Centralized Monitoring Unit (CMU) in Bangalore leads Risk-Based Quality Management (RBQM), ensuring robust oversight of clinical trial data, early risk identification, and mitigation strategies. The organization fosters innovation, collaboration, and excellence in clinical development, while maintaining a patient-centric, inclusive, and purpose-driven culture.

Roles & Responsibilities: • Perform medical review and clarification of trial-related adverse events (AEs) and post-marketing adverse drug reactions (ADRs), including narratives, coding, expectedness, seriousness, causality, and summaries. • Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as per regulatory requirements. • Review coding of AEs, SAEs, SADRs, past medical history, concomitant medications, and other clinical data listings. • Serve as an internal consultant to pharmacovigilance case processing teams on assigned projects. • Perform medical safety review of protocols, Investigator Brochures, and Case Report Forms (CRFs) for safety content and data capture. • Provide aggregate reviews of safety information, including clinical data, post-marketing data, literature, and observational studies (e.g., DSUR, RMP, PBRER, ad hoc reports). • Lead and participate in training, product transitions, audit preparation, and knowledge exchange initiatives. • Review and approve Project Safety Plans and Medical Monitoring Plans per agreed medical safety scope. • Attend project and medical safety team meetings, representing safety and clinical data review findings to clients. • Act as Lead Safety Physician or provide backup support on assigned projects, including 24-hour medical support when required. • Support signal detection efforts and provide medical escalation support for regulatory and safety queries. Qualification: • Medical degree from an accredited and internationally recognized medical school. • Valid medical license or equivalent preferred. Experience: • Minimum 3 years of clinical practice experience post-medical degree. • Minimum 2 years of experience in the pharmaceutical industry preferred, or equivalent combination of clinical and pharma experience. • Knowledge of GCP, ICH guidelines, pharmacovigilance processes (ICSRs and aggregate reports), and departmental SOPs. Skills: • Strong medical knowledge and ability to evaluate safety data. • Experience with multiple safety databases and Microsoft Office (Word, Excel, PowerPoint). • Excellent verbal and written communication skills. • Ability to build and maintain effective working relationships with colleagues, clients, regulatory agencies, and study sites. About the Organisation: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company leverages data, technology, and advanced analytics to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.

Roles & Responsibilities: • Screen and review literature search results (articles, abstracts, citations) for aggregate report inclusion and safety signal detection. • Maintain up-to-date product knowledge to aid literature evaluation. • Support SERM product specialists with ad hoc literature searches. • Ensure timely discussions, escalations, and documentation of safety findings and signal review outcomes. • Identify potential issues and interact with team members to resolve them. • Participate in continuous process improvement initiatives. • Maintain good documentation practice and serve as Point of Contact during inspections/audits. • Build and maintain effective organizational networks. Qualification: • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or related health science. Experience: • Minimum 7 years’ experience in pharmacovigilance, drug safety, literature screening, medical affairs, or clinical research. • Pharmaceutical industry experience preferred, including drug safety, regulatory, clinical development, or medical affairs. • Knowledge of post-marketing regulations and causality assessment principles. Skills: • Strong scientific literature review, data gathering, synthesis, and interpretation skills. • Knowledge of key pharmacovigilance regulations and methodologies. • Excellent written and verbal English communication skills, particularly in scientific/medical terminology. • Ability to evaluate data and draw independent conclusions. • Service-oriented attitude and effective teamwork in a matrix environment. About the Organisation: GSK is a global biopharmaceutical company focused on uniting science, technology, and talent to improve the health of 2.5 billion people by the end of the decade. GSK delivers innovative medicines and vaccines across respiratory, oncology, immunology, HIV, and infectious diseases while fostering a culture of inclusion, patient-centricity, and employee development.

Roles & Responsibilities: • Independently author and review complex clinical and regulatory documents, including protocols, clinical study reports (CSRs), NDA/MAA CTD submission documents, investigator brochures, briefing documents, and regulatory responses. • Ensure high integrity and consistency of data interpretation in all written assignments. • Participate in planning, coordination, and review meetings for document preparation. • Manage 2–3 assignments simultaneously, proactively raising concerns and proposing solutions. • Collaborate with diverse roles within GSK, including Clinical Leads, Asset Leads, Study Delivery Leads, Biostatisticians, and other Medical Writers. • Build and maintain effective communication networks to facilitate smooth cross-functional collaboration. • Adhere to GCP, ICH guidelines, and organizational quality standards for medical writing. Qualification: • Master’s degree or higher in Life Sciences, Pharmacy, Medicine, or a related scientific discipline. Experience: • Up to 5 years of experience in clinical and regulatory writing in the pharmaceutical industry. • Demonstrated experience preparing clinical regulatory documents, including CSRs, clinical summaries, and overviews. • Understanding of clinical trial design, statistical analysis, and interpretation of safety and efficacy results. Skills: • Strong written and verbal English communication skills. • Ability to work in a complex matrix environment and manage multiple priorities. • Knowledge of basic drug development, scientific methodology, and statistical principles. • Familiarity with ICH/GCP guidelines and regulatory submission processes. About the Organisation: GSK is a global biopharmaceutical company focused on discovering and delivering vaccines and medicines to improve the health of 2.5 billion people by the end of the decade. GSK fosters a collaborative, patient-centric culture, combining science, technology, and talent to drive innovation and high-quality outcomes while supporting employee development and inclusivity.

Roles & Responsibilities: • Develop and execute regulatory dossier strategies to meet business and regulatory objectives. • Manage multiple CMC projects and regulatory submissions simultaneously, ensuring timelines and quality standards are met. • Conduct data assessments to ensure dossiers are complete, accurate, and fit-for-purpose. • Identify, document, and mitigate risks related to submission data and information packages. • Escalate critical issues to line management and support resolution. • Review peers’ dossiers, recommend improvements, and contribute to regulatory process enhancements. • Act as subject-matter expert on applicable regulations, guidelines, and procedures for product registration and manufacturing. • Provide consultation, training, and mentoring to colleagues. • Build and maintain relationships with internal stakeholders and external authorities to support project and policy objectives. Qualification: • Bachelor’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or related technical discipline. Experience: • Minimum 5 years of regulatory affairs experience with a focus on CMC for small molecule products. • Practical experience preparing and managing CTD Module 2 and 3 documentation or equivalent quality dossiers. Skills: • Strong project management skills and ability to handle multiple submissions. • Excellent written and verbal communication skills in English. • Ability to draft, review, and present regulatory content clearly. • Knowledge of comparability assessments, change control, stability data interpretation is a plus. • Experience mentoring colleagues and supporting health authority interactions. About the Organisation: GSK is a global biopharmaceutical company uniting science, technology, and talent to improve the health of 2.5 billion people by the end of the decade. With a focus on vaccines and specialty medicines across respiratory, oncology, HIV, and infectious diseases, GSK delivers innovative therapies while fostering a culture ambitious for patients, accountable for impact, and committed to inclusivity and employee development.

Roles & Responsibilities: • Perform medical and scientific data review for hematology clinical trials (e.g., myeloma, lymphoma). • Review standard data listings, adverse events, concomitant medications, patient profiles, and efficacy/safety data. • Support Lead Scientist in medical data review, including protocol deviations, PD analysis, and Medical Review Summary reports. • Collaborate with Medical Directors to develop medical plans (Medical Management Plan, Data Review Plan, Eligibility Review Plan). • Author and review medical data queries, approve query closure, and participate in data review and safety meetings. • Serve as liaison between internal teams, customers, and vendors on medical data and eligibility review. • Collaborate with Clinical Operations, Data Management, Drug Safety, and Project Management to identify data integrity and subject safety risks. • Adhere to ICH/GCP guidelines, data privacy policies, SOPs, and customer-specific procedures. Qualification: • Degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent. Experience: • Relevant scientific experience in clinical trials, medical review, or clinical data management. Skills: • Strong scientific and analytical skills for medical data review. • Excellent written and verbal communication skills. • Proficient in MS Office (Excel, Word, PowerPoint). • Knowledge of drug development, ICH/GCP guidelines. • Ability to manage multiple tasks, prioritize, and work in cross-functional teams. • Self-starter, adaptable to changing priorities and timelines. About the Organisation: Syneos Health is a fully integrated biopharmaceutical solutions organization that accelerates the delivery of therapies through clinical development, medical affairs, and commercial insights. With 29,000 employees across 110 countries, Syneos Health partners with clients to optimize clinical trial outcomes, streamline drug development, and ensure scientific integrity while fostering an inclusive and collaborative work culture.

Roles & Responsibilities: • Coordinate and support remote site activities for assigned clinical studies. • Serve as primary point of contact for site communications, document submissions, and activity coordination. • Support pre-screening, screening, and recruitment activities as assigned. • Manage subject re-consenting, acquire medical records, and conduct protocol activities as directed by the Principal Investigator. • Perform data entry, monitor clinical databases, and respond to system queries. • Maintain documentation in compliance with IRB/FDA policies. • Assist with study closeout and other study-related activities as directed. • Establish and maintain timely communication with sites and collaborate with other Central Study Coordinators. Qualification: • Bachelor’s degree or equivalent experience (minimum 2 years relevant combined experience). Experience: • Experience in clinical study coordination or study team support preferred. • Familiarity with ICH/GCP guidelines and regulatory compliance. Skills: • Strong verbal and written communication skills. • Ability to work independently and collaboratively in a remote setting. • Proficient with web-based research platforms and Microsoft OS environments. • Critical thinking, organization, multitasking, and initiative-taking abilities. • Professional, articulate, and able to maintain confidentiality. About the Organisation: ProPharma Group is a global consulting firm that empowers biotech, medical device, and pharmaceutical companies to advance scientific breakthroughs and introduce new therapies. With expertise across regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma provides customizable, end-to-end solutions to de-risk and accelerate high-profile drug and device programs while fostering a diverse and inclusive workplace.