Trial Site Solutions Director Jobs

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Wolverhampton Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years of clinical research experience, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Leicester Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years experience working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Derby Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Nottingham Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years experience working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Sheffield Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years of clinical research experience, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Leeds Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years experience working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working as a clinical research nurse Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Doncaster Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years experience working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Yorkshire Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years of clinical research experience, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clincal research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Hull Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years experience working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

Job Title: Clinical Research Nurse Banding: Band 5/6 Location: Middlesbrough Hourly Pay Rate: £25 – £30 per hour Join a team driven by one purpose — improving global health outcomes. Our client is looking for a dedicated, NMC‑registered Nurse with at least 3 years experience working in clinical research, supporting innovative clinical trials across multiple therapeutic areas. What You’ll Do Carry out participant visits, observations, interventions and safety checks in line with study protocols and SOPs Complete pre‑screen assessments to support strong patient recruitment Build positive relationships that encourage participant engagement and retention Record, verify and enter study data accurately into source notes and CRFs/eCRFs Respond to data queries promptly Maintain a professional, supportive environment for participants and colleagues Participate in MDT meetings Act confidently in emergencies (e.g., cardiac arrest, anaphylaxis, critical incidents) What you will bring Valid NMC PIN A minimum of 3 years experience working in clinical research Strong clinical experience within a patient‑facing environment Excellent clinical assessment and observational skills Confident communicator with strong organisational skills Ability to work effectively in a fast‑paced research setting High attention to detail and accurate documentation Comfortable using electronic health record systems Apply Today If this sounds like your next step, we’d love to hear from you. Please submit your CV to apply. Why Pulse? At Pulse, you are valued. From the moment you register, our specialist consultants support your career every step of the way. You’ll gain access to exclusive roles through our preferred supplier status, along with ongoing guidance to help you secure the right placement.

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 activities such as implementation of quality control process. Provide medical guidance and expert opinion on the cases to the data entry associates and quality reviewers to help resolve queries. Identify and resolve case issues, coordinate with client therapeutic teams and within functional team and manage as appropriate. Maintain PV expertise and understanding of international safety regulations and guidelines. Responsible for completing the MR activities in the safety database within the stipulated time to comply with service level agreements and regulatory timelines. Provide timely feedback to case processors on the errors/ discrepancies noted. Assist in training/mentoring of other case processing/medical review personnel as necessitated. Adapt to different client case processing conventions and multi-task as per business needs. Perform ad-hoc tasks as advised by the team lead/manager with quality and compliance as per project requirement. Participate in organizational activities to meet objectives suitable for the role/area of expertise. Candidate Profile: Me

Job Title: Specialist Clinical Pharmacist – Acute Care & Oncology Location: Manchester Start Date: ASAP Duration: Permanent Salary: Competitive (dependent on experience, including late shift, on‑call & weekend allowance) Working Hours: 37.5 hours per week, Monday–Friday (part‑time considered) Job Overview Pulse is currently seeking a highly skilled and motivated Specialist Clinical Pharmacist (Acute Care & Oncology) to join an established pharmacy team in Manchester. This is an exciting opportunity to contribute to advanced cancer care and the world’s largest early clinical trials unit. You will deliver high‑quality clinical pharmacy services, supporting oncology and acute care pathways while working within a specialist multidisciplinary environment. Key Responsibilities Provide specialist clinical pharmacy services across oncology and acute care. Support the delivery, evaluation, and continuous improvement of clinical pharmacy services. Act as a clinical role model and contribute to the supervision and teaching of pharmacy, nursing, and medical staff. Support implementation and optimisation of medicine management systems. Contribute to service development, clinical governance, and protocol/guideline implementation. Qualifications and Experience Registered with the General Pharmaceutical Council (GPhC). BPharm, MPharm, or BSc in Pharmacy. Postgraduate clinical qualification (e.g., Diploma in Clinical Pharmacy) essential. Acute hospital experience required. Experience in oncology and/or acute medicine highly desirable. Membership of the Royal Pharmaceutical Society (RPS) desirable. Why Choose Pulse? From the moment you register with Pulse, our focus is entirely on you. Our specialist recruitment consultants understand your profession and are committed to finding the right opportunities to match your skills and aspirations. With exclusive access to roles across the UK, we offer a personalised and supportive recruitment experienc

Overview: Play a vital role in Guidepoint’s success. Guidepoint is seeking an entrepreneurial and outgoing individual to spearhead coverage of our Insights expert call and transcript library product for our Corporate Healthcare client base. As a liaison for our clients and salespeople, you will play a pivotal role in driving engagement and revenue growth within the rapidly expanding Insights product line. Leveraging your exceptional CRM skills, effective organization, and keen attention to detail, you will collaborate cross-functionally to maximize usage of our offering among our active trials and current subscribing clients. This highly visible position will involve working closely with the Insights group heads to develop strategic plans for enhancing client engagement and retention. This is a hybrid role located in New York City. What You’ll Do: Serve as an advocate for the Insights product with corporate healthcare clients and foster three-dimensional relationships with key stakeholders Develop personalized engagement plans for each client depending on therapeutic areas of focus, ongoing clinical trials of interest, and competing companies to effectively market Insights content Monitor and drive client engagement through direct outreach efforts: direct emails, product demonstrations, virtual and onsite meetings Collaborate with sales team to ensure timely renewals and drive upsell opportunities Acquire valuable feedback and insights from clients to inform product development, marketing strategies, and sales efforts What You Have: Bachelors or masters degree from an accredited University, Healthcare-adjacent coursework is a plus 2+ years of professional work experience, with a focus on B2B product sales Understanding of the corporate org structure, the roles, responsibilities, and unmet needs of our corporate buyers, and ability to engage with senior business leaders with innovative content and ideas Excellent communication skill

Overview: Play a vital role in Guidepoint’s success. Guidepoint is seeking an entrepreneurial and outgoing individual to spearhead coverage of our Insights expert call and transcript library product for our Corporate Healthcare client base OR our Institutional Investment/Equity client base. As a liaison for our clients and salespeople, you will play a pivotal role in driving engagement and revenue growth within the rapidly expanding Insights product line. Leveraging your exceptional CRM skills, effective organization, and keen attention to detail, you will collaborate cross-functionally to maximize usage of our offering among our active trials and current subscribing clients. This highly visible position will involve working closely with the Insights group heads to develop strategic plans for enhancing client engagement and retention. This is a hybrid role located in New York City. What You’ll Do: Serve as an advocate for the Insights product with clients and foster three-dimensional relationships with key stakeholders Develop personalized engagement plans for each client depending on areas of focus Monitor and drive client engagement through direct outreach efforts: direct emails, product demonstrations, virtual and onsite meetings Collaborate with sales team to ensure timely renewals and drive upsell opportunities Acquire valuable feedback and insights from clients to inform product development, marketing strategies, and sales efforts What You Have: Bachelors or masters degree from an accredited University, 2+ years of professional work experience, with a focus on B2B product sales Understanding of the corporate org structure, the roles, responsibilities, and unmet needs of our corporate buyers, and ability to engage with senior business leaders with innovative content and ideas Excellent communication skills, with the ability to distill complex issues into clear and concise messages Experience working with or using expert

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