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

Senior Clinical Research Manager - Network Operations

The Senior Clinical Research Manager (CRM) provides strategic and operational ov...

Location

United States , Brookline; Brighton; Milford; Weymouth; Methuen; Foxborough; Londonderry

Salary:

105400.00 - 130500.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor’s Degree required, with a minimum of 7+ years of related experience or Master Degree with 5+ years experience.
Knowledge of cancer as a disease process, cancer treatment modalities, and the clinical trial process.
Experience in protocol development, data compilation and analysis.
Skilled at developing tracking systems to ensure timely data management by the clinical research staff.
Expert knowledge of Federal and State regulations as they relate to research.
Strong interpersonal, organizational and communication skills are required.
Must have computer skills including the use of Microsoft Office and working knowledge of Livelink
EPIC and OnCore applications.
Has expert knowledge of and is fully proficient in ability to execute clinical trials start-up, active and close out phases.
Is fully proficient in their knowledge of clinical research local policy and federal regulation.

Job Responsibility

CLINICAL TRIAL OPERATIONS: Responsible for the oversight of their disease group's clinical trial portfolio and all related regulatory, compliance and performance metrics requirements.
Oversee the processing of protocols through DFCI Institutional Review Board (and other institutions' IRBs) when appropriate.
Collaborate with the DFCI Clinical Trials Office (CTO), the Office for Human Research Studies (OHRS) and the Quality Assurance for Clinical Trials (QACT) to fulfill local and federal requirements governing human clinical trials.
Identify and manage operational, logistical, and regulatory challenges related to the conduct of clinical trials and acts as a leader in overseeing their resolution.
Assist the principal investigator in developing the protocol budget, in collaboration with Research Administration and the Grants and Contracts offices. Work with grant managers and other financial managers in the reporting and accounting of these funds.
Oversees and coordinates the purchase, receipt, inventory and distribution of equipment utilized in the conduct of clinical trials.
Work collaboratively with clinical research administration and grant managers to help monitor and reconcile all study and related grant finances as needed.
Assists the principal investigator in preparing manuscripts for publication.
Collaborate with the DFCI CTO and DF/HCC QACT to develop study forms, database information, and to establish guidelines for monitoring data quality control for PI Initiated studies / Multi-Center Trials
Oversee the subject enrollment, protocol treatment and follow-up care processes for protocol patients.

Fulltime

Director of Research Nursing, Inpatient

The Director of Research Nursing, Inpatient provides strategic, clinical, and op...

Location

United States , Boston

Salary:

215400.00 - 230200.00 USD / Year

Dana-Farber Cancer Institute

Expiration Date

Until further notice

Requirements

Bachelor's and Master's degrees required, one of which must be in Nursing
Registered Nurse with 3-5 years' experience in health care, with progressive administrative experience
Licensed as a Registered Nurse in the Commonwealth of Massachusetts and or New Hampshire as applicable
Exceptional leadership involves mentoring and developing nursing staff, fostering team building, motivation, and a positive workplace culture, while effectively resolving conflicts and facilitating difficult conversations
Strong interpersonal skills enable building relationships across disciplines, with effective communication ensuring clear and compassionate information delivery to staff, patients, and families, and proficiency in facilitating meetings and discussions
Aligning nursing services with organizational goals requires managing multiple priorities, projects, and deadlines efficiently in a dynamic environment

Job Responsibility

Provides strategic, clinical, and operational leadership for all oncology-related clinical trials conducted within the inpatient setting and for some ambulatory research teams
Oversees clinical research operations, ensures adherence to regulatory and ethical standards, and collaborates with physicians, investigators, and interdisciplinary staff to support protocol implementation, patient safety, and protocol integrity through high-quality data collection
Develops and maintains inpatient operational workflows, manages research resources, and drives quality improvement initiatives to enhance trial efficiency and patient outcomes
Serves as a key liaison between ambulatory clinical research operations and inpatient oncology care, fostering a culture of excellence, compliance, and innovation in oncology research
Effective leadership in nursing involves creating a positive work environment through direction and supervision, while implementing strategies to boost staff morale and retention
Building strong relationships with healthcare professionals such as physicians and pharmacists to support integrated patient care
Lead initiatives to implement new programs and technologies that enhances patient care and operational efficiency, with staff engagement being key to successful change processes
Promoting patient-centered care involves initiatives to improve satisfaction and experience, advocating for patient rights, and fostering open communication among staff

Fulltime

New

Patient Safety Manager

Camurus is a Swedish research-based pharmaceutical company committed to developi...

Location

Sweden , Lund

Salary:

Not provided

Life Science Talent

Expiration Date

February 25, 2026

Requirements

Experience within Drug- or Patient Safety/Pharmacovigilance from the pharmaceutical/medical device industry
Background as a pharmacist, nurse or an education within pharmacology or pharmaceutical science
Experience with ICSR/SAE processing, signal detection, aggregate report compilation, and clinical trials
Experience with case processing in safety databases
Experience with database administration of one or more Pharmacovigilance databases
Experience with cross-functional IT projects
Experience with quality processes regarding Change Control and Good Documentation Practice
Knowledge of GVP, regulatory compliance, and quality
Experience with safety database administration
Self-driven, attentive to details, with a proven ability to deliver results in a fast-paced organization

Job Responsibility

Ensure a compliant Pharmacovigilance System for safety surveillance for Camurus products
Support digital surveillance by using data driven methods and approaches
Conduct and drive the digitalisation, automatization, and surveillance activities of safety systems and databases and its life cycle management in accordance with applicable legislation
Drive and lead internal cross-functional teams (Safety, IT Quality, etc.) for safety database projects and activities
Ensure alignment of supplier qualifications, audits, and ongoing performance monitoring activities with the overall strategic activity plan
Ensure adherence to company policies, industry standards, and applicable regulations (FDA, EMA, ICH)
Establish, develop, and maintain strong relationships with key and strategic collaboration with several departments internally to ensure continuous improvement and efficiency, quality, of the safety database and compliance of the activities
Perform review and quality control of ICSRs/SAE and ensure timely submission and exchange of these
Develop the quality system in the area of expertise, as per GVP requirement
Support the QPPV to enable the QPPV to maintain oversight of the Safety database

What we offer

International work environment and corporate culture
Possibility for individual development and growth

Fulltime

Medical Science Liaison

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

Thailand , Bangkok

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Minimum requirement is a degree in Science, or a Clinical Nurse Coordinator or Registered Nurse
5-10 years of experience as Operation Room (OT/OR) Nurse/Scrub Nurse
Be a qualified be a MD, Pharma PhD or PhD in a life science, preferably with specialization and/or clinical experience in the therapeutic area
3 years + of demonstrated success and accomplishment in the pharmaceutical industry.

Job Responsibility

Exchange peer to peer medical and scientific information with customers and internal stakeholders
Be well informed on therapeutic areas, up to date on major studies both ongoing and completed, competitive product information and clinical data
50% focus on supporting the in-house team of Sales and Medical professionals, and 50% of the time focused on KOL and external relations/support
Customer facing position as primary scientific expert in the therapy area(s) and development resource for the therapy team in the region
Maximise patient benefit by expediting the availability of novel treatments and promote the appropriate and safe use of our products
Provides assistance on special projects in the therapeutic area including medical affairs, Animal wetlabs, CMEs, advisory boards, KOL development, Nurse trainings, scientific reviews, Investigators meetings, etc.
Targeting, development and management of key internal and external customers including investigators, site staff, KOLs, government bodies, patient advocacy groups, pharmacists and key medical organisations
Provide scientific support to healthcare professionals
Review of promotional materials to ensure that they meet the legal and scientific standards of accuracy and integrity
Providing product expertise to internal and external customers

Medical Science Liaison

The primary objective of this role is to exchange peer to peer medical and scien...

Location

Thailand , Bangkok

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Minimum requirement is a degree in Science, or a Clinical Nurse Coordinator or Registered Nurse
5-10 years of experience as Operation Room (OT/OR) Nurse/Scrub Nurse
Be a qualified be a MD, Pharma PhD or PhD in a life science, preferably with specialization and/or clinical experience in the therapeutic area
3 years + of demonstrated success and accomplishment in the pharmaceutical industry

Job Responsibility

Customer facing position as primary scientific expert in the therapy area(s) and development resource for the therapy team in the region
Maximise patient benefit by expediting the availability of novel treatments and promote the appropriate and safe use of our products
Provides assistance on special projects in the therapeutic area including medical affairs, Animal wetlabs, CMEs, advisory boards, KOL development, Nurse trainings, scientific reviews, Investigators meetings, etc
Targeting, development and management of key internal and external customers including investigators, site staff, KOLs, government bodies, patient advocacy groups, pharmacists and key medical organisations
Provide scientific support to healthcare professionals
Review of promotional materials to ensure that they meet the legal and scientific standards of accuracy and integrity
Providing product expertise to internal and external customers
Acting with integrity to comply with both local and international regulations, standard operating procedures, processes and corporate governance
Conducting clinical research ethically, efficiently and effectively in order to provide validated data
Develop and implement projects in line with marketing strategies to maximise commercial opportunities

New

Quantitative Researcher Intern

Come build community, explore your passions, and do your best work at Microsoft ...

Location

United States , Redmond

Salary:

Not provided

Microsoft Corporation

Expiration Date

Until further notice

Requirements

Candidate must be enrolled in a full-time Doctorate Degree program in a relevant field (e.g., data science, statistics, behavioral science) during the academic term immediately before their internship
Must have at least one semester or term of school remaining following the completion of the internship
Experience with telemetry, event schemas, and behavioral data analysis
Skills in querying large datasets (e.g., SQL, KQL) and using data analysis tools (e.g., Python, R)
Ability to map user journeys and identify key moments of success or friction
Storytelling and synthesis skills to communicate findings to stakeholders
Comfortable collaborating with cross-functional teams, including UX researchers, designers, and product managers

Job Responsibility

Translate Critical User Journeys (CUJs) and Jobs-to-be-done into measurable telemetry events
Understand and work with event schemas and instrumentation to ensure accurate data collection
Query and analyze behavioral data to uncover insights about user workflows
Define success, failure, and drop-off points within CUJs
Partner with data scientists and other UX researchers to connect telemetry data to user intent and experience
Synthesize findings into actionable insights that inform product strategy

Fulltime

New

Procurement Director

As the Director of Procurement, you will lead the end‑to‑end EMEA / APAC procure...

Location

Poland , Warsaw

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Supply Chain, Engineering, Business Administration, or related field
Master’s degree (MBA or MS in Supply Chain) preferred
10+ years of progressive procurement experience, including 5+ years in a manufacturing leadership role
In‑depth knowledge of major packaging material categories and their cost, performance, and supply‑chain drivers — including engineered and converted substrates
Experience in the pharmaceutical sector is a strong advantage
Strong business acumen and financial analysis capabilities
Purchasing or Supply Chain certification desirable
High proficiency with Microsoft Office (Excel, PowerPoint, Word, SharePoint)
Proven ability to influence, engage, and align senior stakeholders across regions
Excellent presentation and communication skills, with the ability to simplify complex topics for decision‑makers

Job Responsibility

Build a deep understanding of global markets, supplier technologies, manufacturing processes, and cost drivers to anticipate trends and strengthen supply continuity
Serve as a senior advisor to procurement teams and internal leaders, providing strategic insights and market intelligence
Develop and execute global and regional sourcing strategies aligned with business priorities, supplier capabilities, and manufacturing requirements
Drive impactful cost‑optimization initiatives through competitive bidding, advanced negotiations, and proactive supplier management
Negotiate pricing, contract terms, and SLAs
draft and manage contracts as needed
Set clear supplier performance expectations and partner cross‑functionally to evaluate, improve, and elevate results
Lead strategic RFPs and category initiatives that support growth, quality, and margin improvement
Advise R&D and Engineering on supplier capabilities, innovative materials, and emerging trends
Lead risk‑management and supply‑continuity strategies across assigned categories

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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