Our Mission Our passion for improving patients’ lives motivates us to apply our skills, experience and knowledge to advance medicine. We achieve this through flexible, innovative, high-quality solutions for our clients, delivered with integrity. The Role We are seeking a Medical Director to join our Clinical Development team, providing senior medical oversight for complex clinical studies conducted by Simbec-Orion. You will be responsible for ensuring scientific integrity, patient safety, and regulatory compliance throughout the study lifecycle, while acting as Medical Monitor for assigned trials and delivering expert clinical interpretation and safety leadership. You will work cross-functionally with teams including Clinical Operations, Project Management, Pharmacovigilance, Biometrics, Regulatory, Technical Writing, and Business Development to support high-quality study delivery and consistent medical standards across the organisation. In addition, you will contribute strategic medical expertise to proposals, feasibility assessments, and study design, and represent the medical function in client discussions and bid defence meetings, clearly articulating clinical strategy and safety oversight to support successful business development outcomes. Key Accountabilities - Act as Medical Monitor for assigned clinical trials, providing independent medical oversight throughout the study lifecycle. - Serve as the primary escalation point for internal and external stakeholders for all medical and safety issues within assigned studies. - Ensure clinical trials are conducted in compliance with applicable regulations, guidelines, and ethical standards. - Collaborate cross-functionally to support successful study delivery and maintain high levels of client satisfaction. - Oversee the preparation and review of medical and patient narratives and safety update reports to ensure accuracy, quality, and regulatory compliance. - Ensure departmental SOPs are reviewed regularly and updated in line with current regulations, guidelines, and industry best practice. - Contribute to all stages of clinical trial development, including feasibility assessment, protocol and case report form design, investigational site selection, medical monitoring plan development, ongoing medical oversight, adverse event and serious adverse event management, and participation in study-related meetings. - Support business development activities, including proposals, feasibility assessments, site engagement, and bid defence meetings. - Provide therapeutic area expertise across the organisation, including delivery of internal training and review of study protocols and bid proposals. - Lead the resolution of departmental CAPAs and escalations, and cascade relevant audit findings to study teams to ensure appropriate corrective and preventive action. - Ensure timely and comprehensive responses to audit findings and regulatory queries relating to medical and safety matters. - Maintain up-to-date knowledge of developments in therapeutic areas, regulatory requirements, and medical practice relevant to company projects. - Develop and maintain relationships with Key Opinion Leaders and investigators to support study design, patient safety assessment, and business development activities. - Support the Pharmacovigilance function through medical review of ICSRs, CIOMS narratives, and periodic safety reports, identifying and communicating emerging safety trends to project teams and clients. - Provide effective line management to assigned team members, including performance management, objective setting, resource planning, professional development, and ensuring delivery of high-quality work aligned with regulatory, organisational, and study requirements. Skills Required ESSENTIAL - Medical degree with specialisation in Oncology (or equivalent clinical experience in oncology) - Substantial experience as a Medical Monitor within a clinical research environment, with a focus on oncology studies and patient safety oversight - Extensive experience in clinical trial medical oversight within oncology, including adverse event and serious adverse event management, safety signal evaluation, and regulatory compliance - Experience supporting regulatory inspections and audits, including CAPA development and management - Demonstrable involvement in business development activities, including feasibility assessments, protocol input, proposal development, and bid defence participation within oncology trials - Strong commercial awareness, including understanding of clinical trial budgeting and financial drivers within a CRO environment - Strong written and verbal communication skills, with the ability to translate complex oncology data into clear insights for clients and cross-functional teams - Proficiency in electronic data capture systems, safety databases, and Microsoft Office applications DESIRABLE - GMC registered with a licence to practise (or equivalent international registration) with oncology specialism - Pharmacovigilance experience within oncology, including medical review of ICSRs and periodic safety reports - Experience working within a CRO, biotechnology, or pharmaceutical environment with a focus on oncology drug development - Previous experience leading a medical and/or safety function, including direct line management responsibility About Us Simbec-Orion is a responsive and agile full-service CRO, delivering studies from first in man through to Phase III. Our experts leverage wide therapeutic experience and specialist expertise to execute a comprehensive portfolio of trials. We are perfectly structured to provide full-service clinical development solutions for small and mid-size drug developers, headed up by a centralised leadership team. With a focus on tailormade and scalable solutions, we adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients’ lives.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Medical Affairs Group Job Sub Function: Medical Science Liaison Job Category: Scientific/Technology All Job Posting Locations: Madrid, Spain Job Description: Johnson & Johnson Innovative Medicine is recruiting for a Medical Scientific Liaison MSL IMMUNOLOGY – MÁLAGA Are you ready to make a difference? At Johnson & Johnson, we are committed to addressing and solving some of the most meaningful unmet medical needs through creating an environment where our employees feel valued and can reach their potential. This commitment is embedded in our Credo! About the role This is a field-based Medical Affairs position covering the South of Spain. The Medical Scientific Liaison will act as a scientific partner to healthcare professionals, engaging in peer-to-peer discussions that support appropriate clinical use of Johnson & Johnson medicines in Immunology. About Immunology Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases. Learn more at https://www.jnj.com/innovative-medicine The role contributes directly to the local execution of the Medical Affairs strategy by translating scientific evidence into practical clinical dialogue. Through regular scientific exchange, the MSL builds credibility, strengthens relationships with key stakeholders, and supports both short‑term priorities and longer‑term Medical Affairs objectives. The work has a clear focus on improving outcomes for patients living with immune‑mediated diseases. Key responsibilities - The Medical Scientific Liaison develops and delivers an individual activity plan aligned with the country Medical Affairs Plan and relevant Brand Plans. - The role involves maintaining up‑to‑date knowledge of the therapeutic area, treatments, and emerging data in Immunology. - Through planned and on‑request scientific interactions, the MSL communicates balanced and accurate medical information to Leading Specialists and other healthcare partners, in line with approved product information and regulatory standards. This includes participation in medical education initiatives, advisory boards, and scientific meetings at local and regional level. - The role also supports Market Access discussions by communicating objective scientific data to payors and decision‑making bodies, and collaborates closely with internal teams by providing scientific input, training, and support where appropriate. - In addition, the MSL contributes to local medical projects, including studies, registries, investigator‑initiated research, and pre‑approval activities, while capturing insights from the field to inform Medical Affairs planning. All activities are performed in full compliance with pharmacovigilance, healthcare compliance, and company procedures. Qualifications and experience - Candidates should hold a Medical Doctor degree, Pharmacy degree, or a university degree in Natural Sciences or a related scientific discipline. Advanced training or experience in Immunology is preferred. - The role requires solid scientific understanding of the therapeutic area and the ability to analyse and communicate medical data clearly. - Experience in Medical Affairs, an MSL role, clinical research, or a comparable scientific position is expected, along with the credibility to engage in peer‑to‑peer scientific discussions with senior healthcare professionals. - Strong communication skills, the ability to work independently in a field‑based role, and a consistent focus on ethical and compliant conduct are essential. Experience within the pharmaceutical or biotechnology industry, participation in medical education or advisory activities, exposure to payer or Market Access environments, and knowledge of the Spanish healthcare system are advantageous. Additional information - Fluent Spanish and professional English proficiency are required. - The role involves regular regional travel across the South of Spain. - Should hold a valid Driving Licence. - Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: Analytical Reasoning, Analytics Insights, Clinical Data Management, Clinical Trials, Collaborating, Communication, Data Reporting, Detail-Oriented, Digital Culture, Digital Literacy, Execution Focus, Market Research, Medical Affairs, Medical Communications, Medical Compliance, Product Knowledge, Relationship Building, Scientific Research, Technologically Savvy

Employment Type: Full timeShift: Description: Position Summary: The receptionist is responsible for supporting office operations and works independently and interdependently with other office staff to provide efficient, cost effective, quality patient care. Responsibilities include but are not limited to: Promote a healthy work environment Work collaboratively with CNY Family Group Review CCDs for CNY Family Group and route to appropriate team members Collaborate and communicate regularly with management regarding goals, needs/concerns Phone support – Incoming and outgoing phone calls Scanning and faxing documentation General Performance Criteria: · Performs critical job functions that lead to a stream-lined and efficient patient experience · Attention to detail to ensure schedules are accurate based on provider preference sheets and office standards · Meets performance measures in place for each job function and complete job functions by established review date · Works collaboratively with staff and management Communication: · Maintains confidentiality related to patients, family and employees and information specific to service area. · Answers the telephone and routes calls to proper person. When personnel are unavailable for telephone calls, records and delivers messages. · Uses appropriate diction and grammar in conversations. Customer Service: · Employs professional manners and tact in all dealings. Obtains necessary information while remaining courteous about interruptions caused by other calls or events, models calmness. · Customer service orientated. · Adheres to hospital confidentiality statement. Service Specific Skills: · Receives and distributes messages, packages and supplies to the appropriate person or place. · Implements the day-to-day operations of specific service or environment. · Maintains a safe and secure environment. Equipment: · Displays competency related to performing job skills. Including but not limited to: PC terminals, telephones, copier, e-mail system, fax machine Education, Training, Experience, Certification and Licensure: High school graduate or equivalent, business school or formal secretarial training a plus. One to two years’ experience preferred. Participates in orientation and continuing education and updates and maintains knowledge and skills related to specific areas of expertise. Special Equipment, Skills, or Other Requirements: Multi-line telephones, PC and appropriate software knowledge, knowledge of office equipment and supplies. A solid understanding of service-related terminology. Good communication skills both oral and written as well as good interpersonal skills required. Customer service orientated. Work Environment and Hazards: Office setting – exposure Class I or II; service specific. Remote option may be available following training. Training in office for 4 to 8 weeks with the option to shift to remote work. Remote work will stay 100% depending on office needs and productivity Physical Demands: Light work – standing, walking, sitting, and lifting. Work Contact Group: All services, employees, medical staff, patients, visitors, and various regulatory and professional agency staff. Supervised By: Manager or Coordinator Pay Range: $19.00-$23.15 Pay is based on experience, skills, and education. Exempt positions under the Fair Labor Standards Act (FLSA) will be paid within the base salary equivalent of the stated hourly rates. The pay range may also vary within the stated range based on location Our Commitment Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.

This role is for one of the Weekday's clients Job Title: General Medical Officer (GMO) Location: Papua New Guinea Department: Medical – Clinical Experience Required: Minimum 3 years Qualification: MBBS (Mandatory) Salary: PGK 5000- 8000 per month (Net) Job Responsibilities: Deliver comprehensive primary healthcare services to both inpatient and outpatient populations. Conduct thorough patient evaluations, identify medical conditions, and provide appropriate treatments. Track patient recovery and make specialist referrals as necessary. Keep detailed and precise medical documentation while adhering to clinical guidelines. Take part in clinical rounds, case reviews, and healthcare audits. Work closely with nursing and support teams to ensure the delivery of exceptional patient care. Address both routine and emergency medical situations promptly and with compassion. Inform and advise patients and their families about health conditions and preventive measures.