Medical Oncology Consultant - Exeter

Job Description – Medical Writer / Medical Reviewer (Ovarian Cancer Oncology Expertise) Position Title Medical Writer / Medical Reviewer – Oncology (Ovarian Cancer) Location Remote / Hybrid Position Summary We are seeking an experienced Medical Writer or Medical Reviewer with expertise in Ovarian Cancer and Gynecologic Oncology to support the development, review, and delivery of high-quality scientific and medical content. The successful candidate will collaborate with Medical Affairs, Clinical Development, Regulatory Affairs, Biostatistics, and external experts to ensure scientific accuracy, compliance, and timely execution of deliverables. The role requires a strong understanding of ovarian cancer biology, treatment landscape, clinical trial data, and publication practices. Key Responsibilities Medical Writing Develop and review scientific and medical materials, including: Clinical study reports (CSRs) Protocols and amendments Investigator brochures Manuscripts, abstracts, and posters Slide decks and educational materials Medical information responses and FAQs Congress presentations and publication plans Summarize and interpret clinical data related to ovarian cancer therapies and biomarkers. Ensure consistency with ICH, GCP, GPP, and company standards. Conduct literature reviews and evidence synthesis from peer-reviewed journals and congress proceedings. Collaborate with cross-functional teams to support regulatory submissions and medical affairs activities. Medical Review Perform scientific and medical review of promotional and non-promotional materials. Verify scientific accuracy, consistency, and compliance with regulatory requirements. Review clinical data, references, and claims for accuracy and balance. Support MLR (Medical-Legal-Regulatory) review processes. Provide expert input regarding ovarian cancer treatment guidelines and emerging therapies. Scientific Expertise Maintain current knowledge of: Epithelial ovarian cancer Platinum-sensitive and platinum-

ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Senior/ Principal Statistician to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes. SUMMARY The contractor will provide statistical expertise and operational support for oncology clinical trial projects, with responsibility for ensuring the accuracy, quality, and reproducibility of statistical deliverables. The role requires strong oncology clinical trial experience, working knowledge of CDISC standards, and the ability to collaborate effectively with internal study teams and relevant functional partners, as applicable. Key Responsibilities Support statistical analyses of oncology endpoints, including time-to-event and response-based endpoints. Perform event projections to estimate the timing of planned event-driven analyses. Review and provide feedback on SDTM and ADaM specifications, tables, listings, figures, statistical analysis plans, protocol amendments, and relevant study documentation. Conduct routine study data review to identify inconsistencies, missing data, or other issues that may affect analysis or interpretation. Validate statistical outputs and provide documentation supporting reproducibility and quality control. Required Skills and Experience Demonstrated experience supporting Phase 2 and Phase 3 oncology clinical trials, including event-driven and response-based endpoints. Experience reviewing clinical trial data to identify inconsistencies, missing data, unexpected patterns, or issues requiring follow-up. Ability to document review findings, assumptions, queries, and follow-up items clearly and track issues through resolution. Working knowledge of CDISC standards, including SDTM and ADaM. Strong written communication skills, including the ability to summarize findings, recommendations, a

Opportunity At Pulse Doctors , we are proud to be partnering with a leading hospital group in Norfolk to recruit a Substantive or Locum Consultant in Oncology specialising in Lung and CNS Cancers. This is an excellent opportunity to join a well-established oncology team delivering high-quality cancer care within a progressive and patient-focused service. The successful candidate will play a key role in the management of patients with lung and central nervous system malignancies, working alongside a multidisciplinary team of oncologists, surgeons, radiologists, pathologists, specialist nurses, and allied healthcare professionals. The post offers flexible job planning, dedicated Supporting Professional Activity (SPA) time, and the opportunity to contribute to service development, education, and clinical leadership within a supportive NHS environment. Key Responsibilities Provide specialist oncology care for patients with lung and CNS cancers. Deliver outpatient clinics, treatment planning, and ongoing patient management. Participate in relevant multidisciplinary team (MDT) meetings and cancer pathways. Develop and implement personalised treatment plans in line with national and local guidelines. Work collaboratively with colleagues across oncology and wider cancer services to ensure seamless patient care. Contribute to service development, clinical governance, audit, and quality improvement initiatives. Support and supervise junior medical staff and contribute to educational activities within the department. Maintain accurate clinical documentation and comply with NHS, GMC, and Trust standards. Undertake Supporting Professional Activities (SPA) including appraisal, revalidation, teaching, and continuing professional development. Essential Criteria to Apply Full GMC registration with a licence to practise. Entry on the GMC Specialist Register in Clinical Oncology, or eligibility for specialist registration. FRCR (Clinical Oncology) or equivalent recognised

Job Description Job Title: Medical Reviewer Employment Type: Contract Location: Brazil Experience – 2 to 5 Years About ClinChoice ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis. Our global delivery network has expanded to centres and satellite offices in the United States, Mexico, United Kingdom, Armenia, China, Japan, India, and the Philippines to help our customers maintain regulatory compliance locally and globally. We have forged future-defining partnerships with industry bodies and technology companies to develop cutting-edge solutions that deliver our expertise with quality and precision. Primary Responsibilities: Awareness and understanding of relevant GVP modules. Perform medical review of non-serious & serious ICSRs with emphasis on seriousness, expectedness, causality & narrative etc. without missing on quality & compliance. Experience of medical review of ICSRs received from sources such as Spontaneous, Literature, Regulatory Authority, Solicited and Clinical trials. Experience across multiple therapeutic areas such as Oncology, Respiratory, Immunology, Neuroscience, Rare diseases etc. Support triage of cases and determine seriousness and relatedness across products as assigned. Review and verify appropriate selection of adverse events from source documents, assign appropriate MedDRA code, assess labelling and review narrative. Acquire and maintain current knowledge of product portfolio and safety profiles for products across therapeutic areas. Involve in process improvement

🚀 We're Hiring Radiologists | AI Annotation and validation (Remote) We're building the next generation of AI-powered healthcare, and we're looking for experienced radiologists to join us. About the Job Consultant Radiologist 📍 Remote (Work from Anywhere) 🕒 Flexible Hours | Part-Time 💰 Competitive Compensation - Pay per Case Key Responsibilities: 1. Review and validate AI-generated organ segmentations. 2. Annotate radiological abnormalities on CT, Angiography, MRI scans with clinical precision. 3. Assign accurate diagnoses and imaging labels for annotated abnormalities. 4. Ensure high-quality annotations for AI model training. 5. Collaborate remotely with our annotation team via secure platforms. Qualifications: We're looking for an MD/DNB Radiologist with 3+ years of clinical reporting experience. Strong domain expertise in diagnostic imaging (Chest, Cardiology, Oncology, Neurology) Comfortable with digital tools; basic training on annotation software provided. Why Join Us? ✅ Flexible part-time work with competitive compensation that fits around your clinical schedule. ✅ Work remotely from anywhere. ✅ Help build AI that supports radiologists and improves patient care. ✅ Be part of the future of medical imaging and healthcare innovation.

POSITION SUMMARY As the Laboratory Director and one of our Laboratory Directors, you have clinical oversight of Natera’s laboratory testing. You ensure that testing is properly performed, and applicable regulatory standards are met. You are responsible for ensuring that the laboratory implements testing while consistently providing accurate and reliable patient test results. PRIMARY RESPONSIBILITIES: Review, approve, and sign-out reports for a variety of clinical molecular/cytogenetic and/or oncologic results, including NIPT, carrier screening, PGD/PGS, products of conception and oncology testing on platforms including SNP array analysis, NGS, and other methodologies. Oversee the review of genetic and CNV variant data: interpret NGS and microarray results in the context of medical literature, online variant databases and other references along with relevant patient demographic data. Provide clinical and technical support for genetic counselors and other laboratory personnel. Set standards for laboratory testing and acceptable levels of analytic performance and ensure these are maintained. Analyze lab data, contribute to or write publications for high-quality scientific journals. May serve as Clinical Consultant. The Clinical Consultant is responsible for ensuring: Test reports include pertinent information for test interpretation, and Availability for consultation concerning test results and the interpretation of those results as they relate to specific patient conditions May serve as Technical Supervisor. The Technical Supervisor is responsible for ensuring: Appropriate test method selection Adequate method verification to determine the accuracy and precision of the test Enrollment of the laboratory in a CMS-approved proficiency testing (PT) program for the test performed PT samples are tested in accordance with the CLIA requirements PT results are returned within the time frames established by the PT program P