- Medically manage clinical trials to which s/he is assigned as Medical Monitor, serve as Global Lead Medical Monitor (GLMM) for pan-regional and/or global trial(s) to which s/he is assigned; provide after hours medical support for projects to which s/he is assigned
- Provide therapeutic and protocol-specific training to the project teams; contribute medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc.; as directed support Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management; assist in the annual attainment of departmental revenue targets and any other activities as directed by senior management; assist in the mentoring of other medical staff) as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, supports Senior Management's leadership of both the department and the company
- Collaborate with the other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs); demonstrate competence with the execution of SAE related medical review in WORLDWIDEs electronic safety database
- Review and/or assist in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc.,) as directed by senior management; maintain a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc), review of relevant therapeutic/clinical literature and attendance in conferences and meetings; interact with staff in other functional areas within the company to ensure the highest level of client satisfaction through successful execution of projects; identify, document and appropriately resolve out-of-scope work as directed by senior management
- Strong supervision, interpersonal and communication skills as well as conflict resolution skills and be committed to quality and honesty
- Must possess exceptional organizational and planning skills and good documentation skills.
- Must be punctual and have a flexible work schedule.
- In-depth knowledge of the clinical research process, including Good Clinical Practices. Working knowledge of GCPs and regulatory requirements relating to clinical development and safety assure compliance with ethical, legal and regulatory standards. Clinical/therapeutic acumen in medical subspecialty through online and/or in person scholarly programs/lectures
- Able to make good, sound decisions under stress and time constraints.
- A Medical degree (M.D.) with a specialization (board certification) in Internal Medicine or similar field
- At least 2 years of medical monitoring in clinical research or related industry
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Associate Director Immuno-Oncology
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BioTalent London, United KingdomJob Title : Associate Director, Immuno-Oncology · Location : London, UK · About Us: · Our client are a pioneering biotechnology company dedicated to advancing research and developing various solid tumour programs. We are committed to improving the lives of patients worldwide ...
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Associate Director Immuno-Oncology
3 weeks ago
BioTalent Greater London, United KingdomJob Description · Job Title: Associate Director, Immuno-Oncology · Location: London, UK · About Us: · Our client are a pioneering biotechnology company dedicated to advancing research and developing various solid tumour programs. We are committed to improving the lives of patient ...
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Associate Director Immuno-Oncology
3 weeks ago
BioTalent London, United KingdomJob Title: Associate Director, Immuno-OncologyLocation: London, UKAbout Us:Our client are a pioneering biotechnology company dedicated to advancing research and developing various solid tumour programs. We are committed to improving the lives of patients worldwide by harnessing t ...
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Senior Medical Director, Oncology
1 week ago
Worldwide Clinical Trials, LLC United KingdomSenior Medical Director, Oncology - EMEA - Homebased · Requisition Number 7940 · Employment Type : Regular · Who we are · Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical c ...
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Associate Director of Nursing for Oncology
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Royal Surrey NHS Foundation Trust Guildford, United KingdomThe Royal Surrey is a cancer centre of world renown, and the local hospital for the population of Guildford and Waverley. Oncology is integral to the work of the whole trust, and sustaining and expanding the outstanding oncology services we provide is central to the strategy of t ...
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Oncology Market Research Director
3 weeks ago
Oracle London, United Kingdom Full timeCerner Enviza (an Oracle company) is a leading global healthcare consulting firm and trusted advisor to many of the world's top pharmaceutical, biotech, and medical device & diagnostic companies. By supporting the work of Cerner Enviza, you will work with world-class healthcare c ...
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Senior Medical Director, Oncology
3 weeks ago
Worldwide Clinical Trials, LLC United KingdomWho we are · Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in ou ...
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Publication Director- Oncology
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1925 GlaxoSmithKline LLC Brentford, United Kingdom Full timeThe Director, Oncology Publications will lead the establishment of a Strategic Publication Plan in alignment with Global Medical Plans, medical/scientific communication strategy and objectives. In addition, the Global Oncology Publications Director will ensure that specific asset ...
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Proclinical Staffing London, United KingdomProclinical is seeking a dedicated individual for the role of Associate Director, Clinical Data Management. The successful candidate will be responsible for leading the team and overseeing the execution of clinical trials. · Apply promptly A high volume of applicants is expected ...
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Publication Director- Oncology
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GlaxoSmithKline Brentford, Greater London, United KingdomForward to localhost with CLI · whcli forward --token=f97f064b-33b0-4f53-9b9b-f2982f6c9f8c Install whcli · generates free, unique URLs and e-mail addressesand lets you see everything that's sent there instantly. · Built-in integrations: Google Sheets, Excel, Slack, Dropbox, S ...
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AstraZeneca London, United Kingdom Full timeExecutive Director, Oncology Data Science and Translational Medicine Strategy · Location options: Gaithersburg, Maryland, United States | London, United Kingdom · Do you have a strategic mindset , analytical rigor, and collaborative people leadership that enables you to de ...
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Gilead Sciences, Inc. United KingdomSenior Director, Global Oncology Therapeutic Area Safety Physician Senior Director, Global Oncology Therapeutic Area Safety Physician · United Kingdom - Cambridge Pharmacovigilance & Epidemiology Regular Job Description · At Gilead, we're creating a healthier world for all peo ...
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AstraZeneca London, United Kingdom Full timeAre you ready to make a difference in the world of Oncology? We are seeking an Associate Director for our Formulation Sciences team in the TTD chemistry-London group. This role is pivotal in delivering on Formulation strategies for targeted therapeutics, including antibody drug c ...
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Director, RWE – Oncology –
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Taleo BE Uxbridge, United KingdomFor Current Gilead Employees and Contractors: · Please log onto your Internal Career Site to apply for this job. · Job Description · Description: · The Director, Real-World Evidence (RWE)- Oncology will design and deliver RWE required by internal stakeholders and regulators, ens ...
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Clinical Governance Facilitator for Oncology
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Guy's and St Thomas' NHS Foundation Trust London, United KingdomThe main focus of the role will be to focus on the co-ordination of Directorate responsibilities in relation to external accreditation, e.g. ISO accreditation Standards for Better Health; NHS Litigation Authority Risk Management Standards. · 1. Co-ordinate Directorate responsibil ...
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Oncology Medical Co-ordinator
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MSD London, United KingdomThe Business Associate Oncology will support with the Country-to-Country (C2C) HCP engagements coordination as well as be responsible for the day to day administrative and business operations support of the Medical Director Oncology and the wider Oncology Teams. · The Business As ...
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Associate Director, Regulatory Affairs
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Compass Recruitment Solutions London, United KingdomAssociate Director Regulatory Affairs - Oncology Cell Therapy · Cira £150,000 Package · Compass Life Science have partnered with one of the world's leading Biotech's in their search to appoint an Associate Director of Regulatory Affairs focused on Oncology · - Cell Therapy. You w ...
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Personal Assistant
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Guy's and St Thomas' NHS Foundation Trust London, United KingdomAre you a confident team player capable of providing excellent diary management, administration and PA support? Do you have excellent interpersonal skills and enjoy working in fast paced environments? · If that sounds like you, we're looking for a Personal Assistant to help provi ...
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Clinical Governance Facilitator
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Guy's and St Thomas' NHS Foundation Trust London, United KingdomWe have an exciting opportunity for an experienced and enthusiastic governance lead to join the Surgical Oncology directorate team at Guys and St Thomas' NHS Foundation Trust. · As the Clinical Governance Facilitator you will be responsible for delivering the effective management ...
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Imaging & Pathology Co-ordinator
2 weeks ago
Guy's and St Thomas' NHS Foundation Trust London, United KingdomThe Oncology and Haematology Clinical Trials Team (OHCT) is seeking an enthusiastic Imaging and Pathology Coordinator for 12 months Maternity Cover to join our busy team based in Guy's Hospital in Central London. · The successful applicant for this post will work closely with the ...
Senior Medical Director, Oncology - United Kingdom - Worldwide Clinical Trials
Description
Senior Medical Director, Oncology - EMEA - Homebased
Who we are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us What Medical Affairs does at Worldwide Medical Affairs impacts every stage in the lifecycle of a clinical investigation. From Business Development to Regulatory Submissions, members of the MA team support the larger project team, and help establish the medical orientation that characterizes the philosophy here at Worldwide. Activities include direct interactions and presentations with medical and operational personnel from pharmaceutical companies in the process of business development; protocol preparation and country specific feasibility assessments for proposed investigations that inform study design and operational metrics; training of investigative site staff and members of Worldwide project teams on medical or assessment methodology unique to a given study, and the medical monitoring of adherence to enrollment criteria for study candidates as well as medical management activities for patients during the course of the trial. A pharmacovigilance activity for adverse event analyses and reporting is an integral part of the service offering. Medical Affairs also partner with other functional groups within the Worldwide organization for the design and execution of "first in man" studies (CEDRA), the generation of statistical and clinical reports at study conclusion, and scientific/medical assistance in the preparation of regulatory submissions such as investigative new drug applications which permit the initiation of clinical testing. What you will doCreate a job alert and receive personalised job recommendations straight to your inbox.
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