One of our valued Rare Disease Pharmaceutical clients looking for a GCP Drug Development Quality Manager to join the clinical operations team and ensure the smooth running of development projects and QA strategy across multiple functions.The role requires a GCP SME and strong day-to-day quality leader for development projects, taking ownership of QA strategy across pre‑clinical, clinical and regulatory activities. You would build and maintain processes to transfer products smoothly from development to commercial launch, whilst providing supplier and CRO quality oversight, leading audits, managing quality agreements, and holding external partners to organisational standards.You’ll work across multiple therapeutic areas, collaborate with internal teams across the business, and play a key role in strengthening quality systems to support continued growth and unwavering focus on patient safety.Key Responsibilities Serve as Quality Lead for development programs, driving QA strategy across pre-clinical, clinical, and regulatory phases. Partner with cross-functional product development teams to ensure full compliance with quality and regulatory requirements. Develop and implement robust processes to enable seamless transition from development through commercial launch. Provide supplier and CRO quality oversight, including leading audits and managing quality agreements. Act as the Quality representative on cross-functional initiatives, delivering GCP expertise and training. Proactively identify risks, resolve complex quality challenges, and enhance operational quality systems. Key Skills & Experience BSc or MSc in Life Sciences or related scientific discipline. Extensive Quality Assurance experience supporting clinical drug development within Pharma or Life Sciences. Strong working knowledge of GxP and GCP requirements across all phases of clinical development. Excellent written and verbal communication skills with the ability to engage diverse stakeholders. Detail-oriented with strong analytical and problem-solving capabilities. Confident influencer with strong stakeholder management skills and the ability to challenge constructively. Highly organized, dependable, and accountable for deliverables. Demonstrated commitment to compliance, quality excellence, and continuous improvement. Benefits:In addition to being part of a great team and doing things that will make a real difference to patients’ lives, you will enjoy all the benefits that brings: Competitive salaryFlex working – Start earlier, finish earlier and vice versa.A collaborative high performing work environmentPerformance based bonusOpportunity to join a fast growing and ambitious businessCompany pension scheme100% employer paid membership for Private Health InsuranceLife and Critical Illness InsuranceCorporate Gym membershipRegular team building events and an agile working environment If you're an ambitious quality specialist with strong clinical GCP experience and ready for a new opportunity, please send us through an updated resume. Alternatively you can call Freya Peniston-Bird on 020 7959 4302 for further details.

Clinical Site Manager, UK Join a Clinical Operations team supporting the delivery of CRO services for global clinical trials. In this role, you’ll manage clinical study sites from qualification through to ongoing support, helping ensure imaging data quality, regulatory compliance, and effective site coordination across international research projects. Responsibilities Conduct site qualification activities including evaluation, training, and scanner onboarding Manage clinical sites post-qualification, including query resolution Perform imaging quality control (QC) in line with study protocols Act as the main point of contact for assigned sites Track project milestones and maintain site documentation Ensure work is conducted in line with GCP and relevant regulatory standards Looking For 2+ years’ experience in clinical trial site management Experience supporting pharmaceutical or imaging-based studies Familiarity with clinical imaging (e.g. CT or MRI) Strong project management and stakeholder engagement skills Knowledge of GCP and clinical quality standards Experience working within a QMS (desirable) Bachelor’s degree in Life Sciences or related field If you're interested in finding out more, click apply!

 Pharmacovigilance Physician - Oncology REMOTE Competitive Compensation Package Based on Experience SciPro Global is exclusively partnered with an Oncology biotech with promising science that is growing their Safety group as their pipeline progresses. This is the second hire for this group, reporting directly into the Vice President of Safety, and individual who is a calm leader with strong abilitiy to train their team.  Responsibilities include (but not limited to): Safety analysis of both clinical trials & post marketed products.Leading clinical safety aggregate reports such PADERs.Leading risk mitigation and risk minimization measures for global studies, specifically working with RMPs.Responding to health authority queries regarding safety & risk sections of regulatory documents.Perform signal management & lead signal strategy measures.Safety surveillance of all assigned products.Cross functionally act as Safety SME for assigned products & liaise with other Clinical counterparts across the organization.Communicate safety updates with external & internal stakeholders.Provide safety input for clinical study design activities.Identify ways of improvement for team & safety group.  Requirements include (but not limited to): Medical Director or Foreign Equivalent.Minimum 3 years of Pharmacovigilance & Safety experience at a Biotech or Pharma.Oncology Experience required.Management experience.Solution Oriented mindset & motivated!  Are you looking to join a brand name company to grow your career? Apply now to begin the process!