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As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Senior Clinical Data Manager - FSP - fully home-based anywhere in EMEA Joining Fortrea... more ->
Senior Key Account Manager - Cardio-Metabolic - Essex Our client is a rapidly growing, innovative pharmaceutical company that is leading a new paradigm in cardiovascular disease management. They have brought their pioneering cardiovascular treatment to patients in the UK and are recruiting for a talented Key Account Manager at the location shown. Key responsibilities include: Develop Key Account business plans that are cognisant of the strategy for the brand and that drive successful achievement of the territory key deliverables Identify, develop & mobilise KOLs and brand advocates within the... more ->
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. As one of the largest Clinical Research Organizations in the world, operating four ultramodern... more ->
Medpace is currently seeking an office or home based Director of Proposals to join our Clinical Operations team at our London office. The Director will collaborate closely with our medical experts and senior functional managers to create the operational strategy for new business development opportunities. This will include direct management of the proposal team. Responsibilities Mentor/Lead Proposal Writers in the preparation of compelling, strategic proposals, rebids, and exhibits, including rigorous quality control and timeline adherence; Review RFPs, identify any capacity issues, and... more ->
Clinicology Clinicology as part of FGK, is a CRO for the management of clinical and medical device studies. We take pride in our client satisfaction and our collaborative teams, which work as an extension of our client teams. We have successfully run trials across the UK, Europe and beyond, tailoring our clinical research services to meet our client's requirements. Clinicology is a bespoke company that offers speed and flexibility in terms of project start-up and team deployment. Clinicology offers a full range of services including site start-up, monitoring, project management, regulatory... more ->
We are seeking Advanced Nurse Practitioners/Clinical Nurse Specialists with Haematology/Oncology experience who are interested in being at the forefront of new treatments for patients with haematologic and oncologic diseases. This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical research studies (no direct patient care). Experience in the medical management of patients with these diseases, including prescriptive authority, is preferred. Experience in clinical research is preferred. Responsibilities Develop and implement... more ->
Hobson Prior is seeking a dynamic and accomplished professional for the role of Head of Clinical Development. This role involves leading and managing the clinical development team, providing strategic guidance, and overseeing clinical trial data. The ideal candidate will have a strong background in Oncology drug development and clinical research. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Lead and manage the clinical development team, ensuring collaboration with other departments. Participate in or lead the Joint... more ->
Integrated Care Specialist - CV/Metabolic - Cheshire & Merseyside Our client is a family-owned company whose distinctly independent structure means that they are not constrained by the short-term needs of individual shareholders and can focus on the future within long-term strategies of vision and leadership. They have a reputation for providing effective products for the treatment of diabetes, chronic obstructive pulmonary disease COPD, HIV AIDS, Parkinson's disease, Arthritis, and pain relief in Cancer. They are currently looking to recruit an Integrated Care Specialist (ICS) to join their... more ->
Key Account Manager - Urology - NE, NW and NC London This award-winning pharmaceutical organisation was recently voted as one of the Best Companies to Work For due to their very open, people-focused culture and flexible working environment. Their medicines are diverse and include best in class Oncology, Transplantation, Anti-Infective, Urology, Dermatology and Nephrology. With an exciting product pipeline, this company are very sought after and continue to go from strength to strength. This challenging position will require outstanding Key Account Management skill and determination. As part... more ->
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent PhD graduates to enter the industry, receive... more ->
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging/radiopharmaceuticals or/radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management. A fantastic opportunity for recent... more ->
At Charles River, we are passionate about improving the quality of people's lives. When you join our global family, you will help create healthier lives for millions of patients and their families. Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career. As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market... more ->
Integrated Care Specialist - CV/Metabolic - North London Our client is a family-owned company whose distinctly independent structure means that they are not constrained by the short-term needs of individual shareholders and can focus on the future within long-term strategies of vision and leadership. They have a reputation for providing effective products for the treatment of diabetes, chronic obstructive pulmonary disease COPD, HIV AIDS, Parkinson's disease, Arthritis, and pain relief in Cancer. They are currently looking to recruit an Integrated Care Specialist (ICS) to join their team... more ->
We are currently seeking a Manager, Patient Recruitment to join our team within our Clinical Operations group. We are seeking an experienced patient recruitment professional with a background in clinical research and health communications, to join our growing patient recruitment team and support our growth. Responsibilities Develop unique recruitment and retention strategies to manage each study from start to finish Build relationships with Sites through a global site partnership program Adjust to changing study conditions through specialized vendors Qualifications Bachelor's Degree Proven... more ->
This role is a hybrid position which requires a minimum 3 days on-site in Basking Ridge, NJ or Armonk, NY. Remote work is not an option for this role. The Program Operations Leader (POL) will lead and implement the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures... more ->
Overview: This position is to support the Global Patient Safety (GPS) department in business support of safety systems utilized for pharmacovigilance. This includes overseeing daily activities such as generating searches and output in support of departmental data requests, internal audits, and health authority inspections. Additionally, reviewing user requirements for reporting requests (operational and periodic reports such as DSUR, PBRER, etc.), impact assessments and testing reports before releasing to a production state. It also includes project-specific responsibilities, such as... more ->
Reporting to the Global Patient Safety (GPS) Therapeutic Area (TA) Head, the Senior Director, serves as the first point of contact (POC) for all safety related issues for the compound(s) assigned within the therapeutic area (TA). They are the GPS representative on the cross functional Strategic Program Team (SPT) and the Chair of the Safety Management Team (SMT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety profile and the safety strategy. This position requires the... more ->
Position: Project Coordinator Location: Office-based, London Overview: This position will provide extensive training and is suitable for recent graduates; internship, industrial placement, NHS or Clinical Trials experience is also beneficial Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing UK team and engage in clinical trial management on a day to day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company's success. Seeking... more ->
Essential Functions Maintaining an orderly calendar of Pathologist coverage for all assays. Providing Performance Evaluations and on-going feedback to Pathologists on meeting goals and maintaining competencies. Approving absences for illness/vacation. Reporting to Chief Pathologist on strategic goals and routine progress in project delivery, and Determining the need for and executing on employment changes related to hiring/termination/promotion of Pathologist staff. Qualifications Other Medical degree or foreign equivalent at the Licensed Physician level and certification in anatomic... more ->
Hobson Prior is seeking a Clinical Trials Manager to oversee the execution of clinical trials across various therapeutic areas. This role involves managing a geographical region or multiple components of larger studies, typically Phase I studies or other smaller studies. The successful candidate will be responsible for defining and incorporating study logistics and study plans to achieve clinical study objectives and may also participate in strategic initiatives. Responsibilities: Oversee all aspects of small clinical studies, including Phase I studies. Select and manage contract research... more ->