Clinical Trials Pharmacist Job at Hunter Gatherer AHP (London)

Locum Clinical Trials Pharmacist / Pharmacy Technician

Join our NHS client’s team as a Clinical Trials Pharmacist or Technician and tak...

Location

United Kingdom , Dorset

Salary:

24.00 - 31.00 GBP / Hour

Hunter Gatherer AHP

Expiration Date

Until further notice

Requirements

clinical trials experience – this is essential
a current and valid GPhC registration (Pharmacist or Pharmacy Technician)
prior experience supporting or managing research trials in a hospital setting
strong organisational and communication skills
ability to work independently and as part of a multidisciplinary team

Job Responsibility

oversee 15 active clinical trials across renal, oncology, cardiology, and general medicine
support setup and coordination of new clinical trials
supervise and support a junior team member
ensure full compliance with GCP and trial protocols
work closely with both the research and pharmacy departments

What we offer

Fast & simple AHP locum registration
A network of like-minded AHP professionals
Reliable, high-paying locum jobs with bi-weekly payroll
Specialist AHP recruitment consultants
Exclusive NHS & private sector job opportunities
CV marketing & business development support
Industry insights, networking events & discounted CPD

Parttime

Clinical trials pharmacist coordinator

Join a Dermatology Team as a Clinical Trials Pharmacist / Coordinator! A leading...

Location

Australia , Brisbane

Salary:

100000.00 - 120000.00 AUD / Year

Randstad

Expiration Date

March 20, 2026

Requirements

A Bachelor of Pharmacy or equivalent experience
Current unconditional registration with AHPRA
Experience with dispensary and inventory control systems, plus excellent computer and data entry skills
Exceptional verbal and written communication skills for interacting with patients and professional stakeholders
A strong attention to detail and a genuine desire to learn new knowledge relating to clinical research studies

Job Responsibility

Complete patient visits under supervision, including performing ECGs and collecting/processing lab specimens
Dispense and prepare clinical trial medications while managing the drug supply and clinic inventory
Manage scheduling for clinics and trial visit windows to ensure strict compliance
Communicate with Sponsors, on-site monitors, patients, referring doctors, and third-party vendors
Assist in the care of patients on complex drug programs (e.g., biologics), including liaising with the PBS and pharmaceutical representatives
Proactively identify and recruit potential participants for clinical trial programs

What we offer

Gain exposure to cutting-edge treatments before they hit the general market
Flexible working hours, with the usual clinic operations running between 6:00 am and 7:00 pm, Monday to Friday
Comprehensive practice and protocol-specific training

!

Japan Study Manager

Japan Study Managerは、日本国内において治験の管理・監督を担い、CROや治験実施医療機関と連携しながら、治験参加者の安全と福祉、治験の品質を確...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Study management and site management experience
Working knowledge of GCPs, monitoring, clinical and regulatory operations
BS – minimum of 4 years relevant experience
MS/PhD – minimum of 2 years relevant experience
Excellent writing and communication skills in both Japanese and English is required

Job Responsibility

Responsible for in country study/site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and Pfizer standards
Provides quality oversight to the CRO and of the CRO deliverables related to study execution
Leads and coordinates the execution of a clinical trial from study start-up through database release and inspection readiness to ensure timely delivery of quality study data
Provides leadership to the teams in the setting of realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and monitoring plans and for delivery to the agreed plans
Act as core member of the Study Team and will represent the CRO on matters of study execution
Accountable for managing investigator site relationships to ensure effective delivery of clinical trials (e.g., study start up, enrollment, database release), to safeguard the quality of investigator sites (e.g., site health, patient safety) and to maintain investigator and study coordinator engagement and satisfaction
Acts as local expert for the assigned clinical trials and brings that expertise to support the investigator site, which includes the investigator, study coordinator, pharmacist etc, and to oversee and support the site monitor in the conduct of clinical trials
This role is responsible for the resolution of protocol-related issues at the local level
Ensure timely communication with bidirectionally between global and local study team

Fulltime

Coord Pre-Kidney Transplant

Location

United States

Salary:

44.15 - 66.25 USD / Hour

Advocate Health Care

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Nursing or equivalent
5+ years med/surg and/or acute hemodialysis experience which includes 2 years transplant experience
Current RN license in the State of Illinois
CPR certification
Strong analytical skills
Effective at time management
Good organizational skills
Basic computer and database knowledge
Effective communication and presentation skills
Attention to detail

Job Responsibility

Plans, implements and conducts the clinical care of the kidney transplant recipient in the outpatient clinic by coordinating short and long-term follow-up care for patients
Conducts the outpatient clinic two days/week, and as dictated by the needs of the post-kidney transplant recipients
Provides physical and psychosocial support, patient education, wound care, management of hypertension, phlebotomy and general nursing care
Develops a nursing care plan for kidney transplant recipients that include assisting patients with independent management of prescribed medical regimen
Monitors patients to rule out rejection, and documents patient lab results and physical findings, and collaborates with surgeons and nephrologist to provide treatment options
Reviews and interprets patient test results in collaboration with surgeons and nephrologists
Coordinates surgical and diagnostic interventions prescribed by the surgeon and/or nephrologists’ transplant process
Contacts patients (timeliness is essential) at end of clinic visit to review plan of care and make any necessary adjustments in anti-rejection medications
Assists hospital nursing staff in the post-operative care of the kidney transplant.regarding the patients through care coordination and oversight
Assists in the coordination of patient care and the monitoring of nursing care of the kidney transplant recipient through active involvement in treatment planning

What we offer

Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program

Fulltime

Lung cancer MAS team lead

Acts as a line manager leading a team of MAS. Shapes the local strategy and ensu...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Minimum requirement: 4-year university undergraduate degree AND master’s degree in life science, or Pharmacists >4-year university graduates with pharmacist license and master’s degree or equivalent life science research experience, or >6–year university graduates with pharmacist license, or Nurses with a master’s degree, or Veterinarians, or Dentists, or MDs
Preferred: MD (clinical experience, board certification preferred), or PhD in Life Science
Experience in the pharmaceutical industry, preferably as a Medical/Scientific Advisor, MSL, team lead, and/or clinical experience with direct patient care and/or professional experience in the pharmaceutical industry in relevant areas
MA/DJ experience and / or research experience preferred
Scientific publication
Strategic Thinking: Ability to consider the direction of Medical from a mid-to-long-term perspective and formulate strategies as a manager at Pfizer
Communication Skills: Ability to conduct clear and efficient communication, including with other departments, and convey information accurately and logically
Decision-Making Ability: Ability and responsibility to make quick and effective decisions even in situations where there is no clear answer
Leadership: Ability to influence teams and departments and drive them towards achieving organizational goals
Financial Skills: Ability to manage budgets and execute actions reliably and on schedule

Job Responsibility

Acts as a line manager leading a team of MAS
Shapes the local strategy and ensures the delivery of scientific-medical expertise and exchange with KOLs in the assigned therapeutic area
Lead the Pfizer Japan medical scientific point of contact for HCPs, medical societies, regulators, academia and other external stakeholders
Play a central role as a scientific and medical leader who can identify unmet medical needs(UMRs), drive the building and executing medical plans and oversee establishment of clinical evidence
Demonstrate medical and scientific leadership and expertise
Ensure and oversee the highest scientific standards during in / external activities to provide deep medical and scientific expertise
Lead development of local medical plan aligned with global medical plan to address local UMRs and fill data gaps, and manage implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines
Direct and supervise providing and exchanging medical/scientific information for/from medical facilities in the assigned area and external stakeholders and make strategic decisions on medical strategies for assigned products
Drive and monitor heightened understanding of the burden of disease in the assigned therapeutic area and medical attributes of our products to enhance the safe and efficacious use
Lead achievement of department/team goals, and/or manage cross-organizational projects, providing guidance and accountability for results

Fulltime

Hcp liaison manager

Talentmark are working in partnership with a leading UK life sciences biotechnol...

Location

United Kingdom , London

Salary:

55000.00 - 70000.00 GBP / Year

CK Group

Expiration Date

Until further notice

Requirements

MPharm
PhD qualified in virology
Proven experience in a comparable field-based role, with a track record of building and leveraging a network of HCPs to support volunteer/patient recruitment
Strong scientific understanding, enabling confident discussion of clients’ clinical trials with healthcare professionals, including GPs, specialists and pharmacists
Hold entitlement to work in the UK

Job Responsibility

Proactively identify, engage and formalise partnerships with HCPs — including GPs, consultants, pharmacists and patient advocacy groups — to drive patient identification and enrolment
Lead educational initiatives
Support marketing strategy development
Work cross-functionally to achieve recruitment objectives
Develop and maintain a network of contracted HCPs and partner organisations to drive patient recruitment
Provide strategic insights to inform business development proposals and study planning activities
Take full ownership of event delivery, including agenda development, speaker coordination, logistics and budget oversight
Work closely with internal teams and marketing to ensure effective and impactful execution
Represent the organisation at conferences and coordinate stakeholder engagement events
Contribute to the development and dissemination of patient recruitment materials

Fulltime

Director, Operations CMSU

To direct, oversee and coordinate all aspects of the Clinical Material Services ...

Location

United States of America , Rochester

Salary:

108483.00 - 162725.00 USD / Year

University of Rochester

Expiration Date

Until further notice

Requirements

BS degree required
Doctorate degree in pharmacy and Business administration background, preferably with an MBA preferred
3 years of relevant experience required
15 + years’ experience in the pharmaceutical industry with strong working knowledge of FDA compliance, including cGMP and clinical supplies preferred
Minimum of 8 years proven leadership, supervisory and people management experience preferred
Strong working relationships with executives in the clinical trial supply and pharmaceutical industries required
Experience contracting with and managing contract vendors
Strong working knowledge of investigational drug handling and distribution as well as the conducting and design of clinical trials
Strong organizational and communication skills required
Strong computer skills required

Job Responsibility

Direct the Clinical Supplies Operations Group
Responsible for all aspects of drug/device supply operations
Management of CMSU Operations Personnel
Oversee team and ensures that the CMSU facilities and equipment remain in full compliance with all NYS, Federal, and ICH regulations
Work in collaboration with CMSU Leadership and Project Manager to provide input and oversight in creation of study specific Clinical Material Specification Sheets (CMSS) and process orders (PO)
In conjunction with the CHET Financial Leadership and CMSU Leadership, develop the CMSU operational budget and assist and managing to it
Responsible to ensure that the CMSU’s time and effort is accurately reported by project to the CHET finance team for billing to each project
Work in close collaboration with the Quality Assurance Group
Responsible for ensuring regulatory compliance with investigational drug/device regulations and actively supporting IND submission for internal/external clients with focus on the Chemistry, Manufacturing and Control (CMC) section of the IND

Fulltime

Medical Director of Liver Transplantation

Lead a nationally ranked transplant program with exceptional academic support an...

Location

United States , Milwaukee

Salary:

430000.00 - 530000.00 USD / Year

American Society of Transplantation

Expiration Date

Until further notice

Requirements

BC/BE Transplant Hepatologist
Doctorate Degree
2 - 5 years experience

Job Responsibility

Serve as Medical Director of Liver Transplantation
Lead collaborative program development within the Medical College of Wisconsin transplant service line
Direct provider engagement and program growth through accountable care initiatives
Mentor trainees in a fully accredited GI & Hepatology Fellowship with a planned Transplant Hepatology Fellowship
Receive protected time and funding to pursue clinical trials, QI projects, and translational research
Access research support through the Clinical Trials Office and CTSI coordinators
Practice in the new Digestive Disease Center opened in 2024 with cutting-edge facilities
Access a full complement of APPs, nutritionists, pharmacists, and advanced endoscopy capabilities
Join a nationally ranked multi-organ transplant service line with excellent outcomes
Expand patient population through outreach opportunities across Wisconsin

Fulltime

Clinical Trials Pharmacist

Hunter Gatherer AHP

Location:
United Kingdom , London

Category:
Pharmacy

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
July 05, 2025

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