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Student placement - medical writing and pharmacovigilance assistant

Stratford-upon-avon
Cancer Research Uk
Medical writer
Posted: 28 October
Offer description

.**Student Medical Writing Assistant and Pharmacovigilance Assistant**£23,000 plus**Reports to:** Principal Medical Writer**Directorate:** Research & Innovation**Contract:** 54 Weeks Fixed Term Contract**Hours:** Full time 35 hours per week**Location:** Stratford, London Office-based with high flexibility (1-2 days per week in the office)**Closing date:** 02 November 2025 23:55This vacancy may close earlier if a high volume of applications is received; therefore. we strongly recommend that you apply early to avoid disappointment. Please let us know if there is anything about the recruitment process that you would like to discuss, in particular if there are any changes or adjustments that would make it easier for you to apply. Please contact recruitment@cancer.org.uk or 020 3469 8400 as soon as possible.**Visa sponsorship:** You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is **not** able to offer visa sponsorship.**Recruitment process:** Competency based interview + written task in relation to the placement**At Cancer Research UK, we exist to beat cancer.**Cancer Research UK are looking for a motivated and ambitious undergraduate student to join our Centre for Drug Development (CDD) as Student Medical Writing Assistant and Pharmacovigilance Assistant. To find out more, read all details below; you can also hear from some of our past students (click ).**About the placement**The CDD at Cancer Research UK consists of a diverse and experienced office-based and home-based team who sponsor and manage high quality early phase clinical trials. We work in collaboration with leading scientists and clinicians around the UK to develop effective new anti-cancer treatments.Here at the CDD, we’re offering a unique opportunity to gain valuable experience and training within a world-class clinical research environment. Our placements will provide you with an exciting opportunity to develop key skills, which will help to open doors to future careers within this industry. During this placement year, the chosen candidates will be provided with training, mentorship, and exposure to key roles in drug development and pharmaceutical research.If you’re a motivated life sciences student, with an interest in drug development and oncology clinical trials, then this is your opportunity to gain invaluable experience working within the pharmaceutical sector.We have one 54 week placement to offer, with negotiable start date in July 2026.This role will be split between the Medical Writing and Pharmacovigilance teams, and will include the following responsibilities:* Provide administrative support to the Medical Writing and Pharmacovigilance teams as required.* Support other functions in the Quality, Regulatory, Pharmacovigilance and Medical Writing (QRPM) department with administrative tasks where appropriate.* Build good working relationships with key functions in the CDD to ensure timely delivery of documents.* Organise meetings (either online or in-person) with both internal and external groups, taking minutes as requested.* Support the Medical Writing and Pharmacovigilance teams in maintaining relevant sections of the Trial Master File, ensuring that documentation is filed and reviewed appropriately.* Develop and maintain an awareness of the main clinical development activities, in particular those related to the QRPM department.* Develop and maintain an awareness of CDD clinical trials and key projects.* Other tasks delegated by the Principal Medical Writer or Pharmacovigilance Manager.**Pharmacovigilance****:*** Assist with data entry of serious adverse event information from Investigator sites related to adverse event reporting;* Assist in obtaining further information from Investigator sites related to adverse event reporting.**Medical writing:*** Manage and track documents required for Clinical Study Report (CSR) and Investigator Brochure (IB) preparation;* Provide support for the preparation, authoring, review and quality control of CSRs, safety narratives, report appendices, IBs, lay summaries of results, and other documentation as required.## If you’re a motivated life sciences student, with an interest in drug development and oncology clinical trials, then this is your opportunity to gain invaluable experience working within the pharmaceutical sector. You will need to be able to demonstrate:* Strong organisational and time management skills;* Excellent communication skills (written and verbal);* Ability to confidently communicate with an array of internal and external contacts. Excellent attention to detail;* Ability to work as part of a team and independently in an enthusiastic, proactive fashion;* Good working knowledge of Microsoft based packages (Word, Excel and Powerpoint);* Strong problem-solving skills;* Familiarity with ICH/GCP guidelines would be beneficial but isn’t essential (you will learn in the role);* Experience working in an office environment would be beneficial but isn’t essential.Please read the following information carefully before applying:If you would like to apply for the placement student scheme, please ensure that you meet the following criteria before completing your application form:* You must be currently studying for an undergraduate degree at university. Your degree course must support a placement year in industry. Please note that applications from graduates or PhD students, or students for whom a placement year is not a part of their degree course, will NOT be considered for this scheme.* You should expect to receive a 2:1 or grade B in your year-end results in a science related degree.* You should have 3 A levels (or equivalent) grade B and above (preferably one in a biological science).* You should be able to commence work in July 2026 (the start date is negotiable).* You should have the right to live and work in the UK without restriction. We regret that we cannot consider applications from candidates who require a work permit to work in the UK.If you meet these requirements, we look forward to receiving your application.Please note that this role is flexible role (office-based with an option to partly work from home), **not laboratory based.**Useful tips for completion of the application form:* Read through the whole form first and draft your answers accordingly.* Complete all sections - please do not leave any gaps.* Check your spelling and grammar.* Be concise and focused in your answers.* And finally, don’t forget, it’s important that you tell us how you found out about the scheme.If your application is shortlisted, you will be invited to attend an interview (likely to be virtual). This will involve some exercises designed to assess your ability and a competency interview. If we have a large number of applicants then a short screening call may precede the main interview.We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form and answer some screening questions for us to be able to assess you fairly and objectively.Our organisation values are designed to guide all that we do.**Bold:**Act with ambition, courage and determination **Credible:**Act with rigour and professionalism **Human**: Act to have a positive impact on people **Together:**Act inclusively and collaborativelyWe’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.## We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and
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Home > Jobs > Healthcare jobs > Medical writer jobs > Medical writer jobs in Stratford-upon-avon > Student Placement - Medical Writing and Pharmacovigilance Assistant

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