PROCLINICAL is looking for employees for positions:
clinical scientist
Trade
media & Communications
Media & Communications
Responsibility
accountable for keeping updated on the alterations in GCP and updating the division on any changes
guide and offer clinical scientific knowledge for the design, planning and implementation of clinical trials
guarantee all written documents are clear, scientifically precise and in compliance with regulatory guidelines
work alongside other divisions to offer scientific contributions and writing knowledge
you will interface with clinical operations to guarantee clinical trials are implemented effectively and in compliance with applicable guidelines
produce, track and handle project budgets and timelines with the capacity to offer comparison updates on financial accruals versus projects budgets
supervise and analyse clinical data, to guarantee the quality and integrity of clinical data and that trials are performed rendering to both protocol and scientific standards
other duties may be assigned to this role
Requirements
educated to an advanced degree level in a connected scientific field would be ideal
demonstrable experience in clinical research or clinical development, ideally in a biotech or pharmaceutical organisation
familiarity with psychiatry or neurology would be ideal
acquaintance with phase 2b clinical trials and a comprehension of the drug development procedure
medical writing abilities with a background in producing high quality clinical documents
past involvement using regulatory guidelines linked to clinical development and medical writing
an organised individual with the ability to resolve issues
communication skills both verbally and in writing
structural design engineer
Working hours
permanent
Responsibility
offer examinations and suggestions regarding suitable loads and loading conditions
possess expertise on pertinent forming codes and present standards that influence structural design results
discuss proposed design solutions to crucial shareholders
proclinical are recruiting for a Senior Structural Design Engineer to join a biopharmaceutical organisation. This role is on a permanent basis and is has multiple UK locations
contribute to the initial planning stages to present structural solution alternatives for the design team and he end client's needs
other duties to be assigned
implement contemporary design and modelling practices to examine materials and connections, taking into consideration factors, for example: strength, durability, feasibility, and cost-efficiency
Requirements
demonstrated acquaintance with cleanroom design, ideally within a GMP/ISO regulated pharmaceutical cleanrooms
educated to a degree level in a civil engineering, structural engineering or any other pertinent building design field
familiarity with Revit and AutoCAD
comprehension of BIM tools and software
computer literacy
expertise on working to FDA/ISO/GxP standards would be ideal
an organised individual with the ability to resolve issues
communication skills both verbally and in writing
maintenance manager
Working hours
permanent
Responsibility
arrange vendor-connected upkeep actions which involves, scheduling, contractor safety training and work permits
support the evaluation and processing of vendor calibration and maintenance certificates and service reports
uphold and produce CMMS asset information, SOPs, and work records
aid quality management systems linked actions such as audits, investigations, deviations, CAPAs, etc
proclinical are recruiting for a Maintenance Planning Manager to join a pharmaceutical organisation. This role is on a permanent basis and is located in Oxford
produce and uphold calibration and maintenance schedules and work records for all facility utility systems and equipment
administer computerised maintenance management system for planning, scheduling and reporting for all upkeep and calibration-linked actions
other duties may be assigned to this role
Requirements
educated to a degree level or similar
at least 5 - 7 years of experience with maintenance planning and CMMS would be ideal
at least 2 - 4 years of experience with applicable GxP would be desirable
computer literacy
communication skills both verbally and in writing
an organised individual with a high attention to detail
works well independently
capable of performing tasks in a timely manner
brand manager
Working hours
permanent
Responsibility
proclinical are recruiting for a Senior Brand Manager to join a pharmaceutical organisation. This role is on a permanent basis
accountable for handling A&P budget
train a high performing cross-functional brand team
contribute into international product method via partaking in international brand teams
compete full alignment around the brand method and implementation with internal cross-functional shareholders
assist with tender proposals to guarantee high quality, cross-functional approved responses
you will use disease and market comprehension to develop customer acumens, novel concepts, and brilliant planning to implement commercial methods
guarantee consistency of the brand actions and methods with the portfolio/brand method
Requirements
an organised individual who is a result driven and dynamic person
capable of thinking analytically
able to form relationships and work well with others
A motivated individual with the ability to prioritise and plan well
educated to a degree level or higher
at least 8 years of experience working in a pharmaceutical marketing setting
familiarity with product launches and with multichannel marketing
presentation abilities
technical writer
Working hours
permanent
Language
english
Responsibility
proclinical are partnering with a CRO who are currently recruiting for an individual to join their team
this role is on a permanent basis with the ability to work remotely from anywhere in Europe
the opening position is for a CMC Technical Writer - Vaccines/Biologics
supervise the supportive data offered by any other divisions that are compliant
guarantee that the arrangement with the other divisions will be included in the authoring/evaluation procedure
author and assist the regulatory affairs
other duties may be assigned
handle and schedule with SMEs and site conformance, which also involves production, validation and quality assurance, to author/evaluate procedure to guarantee accomplishment in a timely manner
Requirements
familiarity with authoring CMC parts of regulatory documents such as registration files or variations
knowhow of regulatory processes/systems/directions
acquaintance with biologics or vaccines
expertise on qualification/validation principles
able to manage own time efficiently to meet targets
able to think analytically, creatively and critically
communication skills both verbally and in writing
proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies
software developer
Responsibility
accountable for the design, development and upkeep of software applications across a varied technology portfolio
you will assist with testing, debugging, and processing the applications to generate the necessary product
other duties may be assigned
proclinical are recruiting a Software Developer for a pharmaceutical organisation. This role is on a contract basis and is located in London
Requirements
capable of approaching issues head on and resolving them
able to support the preparation of both program-level and user-level documentation
works well under minimal guidance
possesses pertinent skills and knowledge for the role
proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies
proclinical Staffing is an equal opportunity employer
events coordinator
Responsibility
handle the expectations of all parties and mediating with third party providers
gather and offer post-event feedback, finalising budgets, and invoices which is crucial for the success of future events
arrange a large internal kick-off event in January 2023
proclinical are recruiting an Events Coordinator for a pharmaceutical organisation. This role is on a contract basis and is located in London
the ideal candidate will arrange registration, allocate assistance, and onsite actions
other duties may be assigned to this role
you will handle various events and customer visits simultaneously as well as daily tasks that involves raising purchase orders, reconciling expenses, and arranging customer transport
Requirements
past involvement in and know-how of running virtual, hybrid and in-person events
computer literacy
familiarity with project and shareholder management tasks
an organised individual with the ability to manage time efficiently
proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies
proclinical Staffing is an equal opportunity employer
comprehension of and thriving in the vision of the events team, apricating the company's organisational priorities and needs to guarantee that all is constantly generated to the highest standards
validation engineer
Working hours
permanent
Responsibility
proclinical are recruiting a Validation Engineer for a biotech corporation. This role is on a permanent basis
accountable for qualification protocol and report production, which involves acceptance criteria production
evaluate, revise and accomplish documentation rendering to cGMP
form, revise and uphold validation plans and processes for qualification of equipment needed for cGMP compliance
support the troubleshooting equipment/system failures and impact examinations
engage with cross functional groups as well as internally to discuss validation needs and progression updates
handle vendors and contractors conducting qualification actions
arrange scheduling, implementation and evaluation of qualification protocols/reports
Requirements
educated to a degree level or various years of pertinent engineering work experience
familiarity with equipment validation to assist with QC testing, which involves temperature mapping
comprehension of pertinent industry guidelines/regulations for equipment validation
know-how of cGMP and GDP needs
A high attention to detail
capable of resolving issues
communication skills both verbally and in writing
proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies
senior account manager
Working hours
permanent
Requirements
previous involvement working within an international agency collaborating with a pharma organisation on product and methodical marketing communications
familiarity with cardiovascular, oncology, metabolic, rare disease, etc
acquaintance within an advisory board, HCP and PAG shareholder management role
capable of advocating for the patient always
communication skills both verbally and in writing
A creative individual with media skills
works well with others
able to resolve issues
Responsibility
other duties may be assigned to this role
chronic kidney disease - improve diagnosis, tracking and treatment for patients on an international level to reduce the risk of having to go on dialysis or receive a transplant or death
full stack developer
Working hours
permanent
Responsibility
support the Director with project tracking/contribution and upkeep
look for and refine new and novel approaches, solutions, and prospects to improve project effectiveness, outcomes or team performance
guarantee project delivery timelines/deliverable expectations are met
you will meet deadlines and accomplish goals through efficient management of workload, company and prioritisation
offer contributions to assist the Director with budget revisions, and reconciliations to guarantee budget precision
the ideal candidate will accomplish projects with a focus on client satisfaction in an effective and timely manner
collaborate with the specialist/senior specialist in the digital team to offer routine prediction updates for all allocated projects
other duties may be assigned to this role
Requirements
educated to a degree level in a business development field with experience in an account management role in a pharmaceutical organisation
know-how of HTML5, such as JavaScript, CSS and HTML
advanced expertise in JavaScript which involves jQuery
experience with AJAX and JSON database connectivity and integration
acquaintance in a client-facing position
prior involvement working within a Healthcare, CRO, Pharmaceutical Industry, Client or MedComs Agency
at least 5 years of experience in digital engagement
A flexible, driven individual with an open mind on digital innovation