5 jobs found in Maidenhead, Berkshire

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    • maidenhead, berkshire
    • temporary
    • £40,000 - £45,000 per year
    • full-time
    JOB TITLE: Regional Commercial Operations AnalystDURATION: 6 Months (Extensions)LOCATION: Maidenhead (Office based)PAY: £40 - £45K Per Annum Your potential new role The Regional Commercial Operations Analyst is responsible for driving sales operations and value creation activities within a region. This is a fantastic opportunity to work for a world leading multinational medical device company. Major Accountabilities Proactively monitors and strives to maintain high levels of quality, accuracy and process consistency in the regional organization's planning efforts. As needed, coordinates planning activities with other functional roles.Responsible for Regional data- and insights-driven problem-solving exercises, as required. Includes integrating data from multiple sources (e.g. Salesforce.com, IBM Cognos, etc.), identifying solutions for the enablement of business priorities, and driving the execution.Manages proactively all instrument planning forecasts and drives asset management of existing inventory.Coordination of all Salesforce.com activities: driving Salesforce.com adoption, usage, and accuracy; managing Regional Salesforce.com support tickets; managing Regional customer data hierarchy; primary contact for allSalesforce.com related needs across the Regional organization.Assists Regional management organization in understanding process bottlenecks and inconsistencies. Facilitates an organization of continuous process improvement. What we are looking forMinimum of 3-5 years of experience, with a focus on insights-driven problem solving and decision making.Must be proficient in Microsoft Office suite of applications and demonstrate a mastery of Excel. Familiarity with Power BI a plus.Experience using varied data sources a plus, including Microsoft Access, IBM Cognos servers, and Salesforce.com reporting tools.Must be team-orientated, analytical, and highly organized. Results Driven - confident, thrives on hard work and consistent challenge and is quick on his/her feet. Monitors quantitative progress measures and acts quickly on deviations from plan. Consensus-building - capable of utilizing strong interpersonal, verbal, presentation and writing skills to successfully interact with subordinates, colleagues and executive management.Team Oriented - builds strong relationships, is a strong motivator who knows how to influence, and overcomes barriers within own organization, peer organization, and virtual organization.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    JOB TITLE: Regional Commercial Operations AnalystDURATION: 6 Months (Extensions)LOCATION: Maidenhead (Office based)PAY: £40 - £45K Per Annum Your potential new role The Regional Commercial Operations Analyst is responsible for driving sales operations and value creation activities within a region. This is a fantastic opportunity to work for a world leading multinational medical device company. Major Accountabilities Proactively monitors and strives to maintain high levels of quality, accuracy and process consistency in the regional organization's planning efforts. As needed, coordinates planning activities with other functional roles.Responsible for Regional data- and insights-driven problem-solving exercises, as required. Includes integrating data from multiple sources (e.g. Salesforce.com, IBM Cognos, etc.), identifying solutions for the enablement of business priorities, and driving the execution.Manages proactively all instrument planning forecasts and drives asset management of existing inventory.Coordination of all Salesforce.com activities: driving Salesforce.com adoption, usage, and accuracy; managing Regional Salesforce.com support tickets; managing Regional customer data hierarchy; primary contact for allSalesforce.com related needs across the Regional organization.Assists Regional management organization in understanding process bottlenecks and inconsistencies. Facilitates an organization of continuous process improvement. What we are looking forMinimum of 3-5 years of experience, with a focus on insights-driven problem solving and decision making.Must be proficient in Microsoft Office suite of applications and demonstrate a mastery of Excel. Familiarity with Power BI a plus.Experience using varied data sources a plus, including Microsoft Access, IBM Cognos servers, and Salesforce.com reporting tools.Must be team-orientated, analytical, and highly organized. Results Driven - confident, thrives on hard work and consistent challenge and is quick on his/her feet. Monitors quantitative progress measures and acts quickly on deviations from plan. Consensus-building - capable of utilizing strong interpersonal, verbal, presentation and writing skills to successfully interact with subordinates, colleagues and executive management.Team Oriented - builds strong relationships, is a strong motivator who knows how to influence, and overcomes barriers within own organization, peer organization, and virtual organization.Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    • maidenhead, berkshire
    • contract
    • £40.00 - £48.00 per hour
    • full-time
    Responsible for all local Pharmacovigilance-related activities for provision of safety report handling relating to Development and maintenance of local PV processes and procedures.As Drug Safety Manager, you will: Reviewing local and national legislation (MHRA or HPRA) to maintain an awareness of local regulations and ensuring local processes are aligned Notifying Global Drug Safety of any programmes/contractual arrangements with external providers with significance for handling AE information Monitoring the MHRA portal for safety reports To be considered for the role of Drug Safety Manager, you will:At least 5 years experience in Drug safety/ Pharmacovigilance in a Pharmaceutical business2 Years in PV Affiliate functionDrafting and Revising safety detailsextensive PV affiliate experience beyond just ICSR managementRSG Database 12 Month Contract, full time. This is an Inside IR35 role, based in Maidenhead. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    Responsible for all local Pharmacovigilance-related activities for provision of safety report handling relating to Development and maintenance of local PV processes and procedures.As Drug Safety Manager, you will: Reviewing local and national legislation (MHRA or HPRA) to maintain an awareness of local regulations and ensuring local processes are aligned Notifying Global Drug Safety of any programmes/contractual arrangements with external providers with significance for handling AE information Monitoring the MHRA portal for safety reports To be considered for the role of Drug Safety Manager, you will:At least 5 years experience in Drug safety/ Pharmacovigilance in a Pharmaceutical business2 Years in PV Affiliate functionDrafting and Revising safety detailsextensive PV affiliate experience beyond just ICSR managementRSG Database 12 Month Contract, full time. This is an Inside IR35 role, based in Maidenhead. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    • maidenhead, berkshire
    • contract
    • £30.00 - £40.00, per hour, Depending on experience
    • full-time
    My client, a leading Pharma Biotech, has a requirement for an experienced Medical Info Associate to join their business at their Maidenhead facility on a 6 Month Contract. As Senior Medical Information Manager, you will:Assisting with the collection and reporting reports of all adverse events/product complaints as defined both by internal SOPs and UK/Irish regulationsCopy approval review/approval for factual accuracy of promotional and informative material through VeevaEnsure all promotional material adheres to both the ABPI Code of Practice and the Medicines Act IPHAReviewing/approving promotional and informational material in line with approved product labellingTo be considered for the role of Senior Medical Information Manager, you will: Educated to degree level in a relevant scientific field Minimum of 3 years industry experience Experience in handling 2nd line MI enquiries and generating standard responses Ability to understand technical, scientific, and medical information Experience of working in Neurology and/or immunology preferred Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    My client, a leading Pharma Biotech, has a requirement for an experienced Medical Info Associate to join their business at their Maidenhead facility on a 6 Month Contract. As Senior Medical Information Manager, you will:Assisting with the collection and reporting reports of all adverse events/product complaints as defined both by internal SOPs and UK/Irish regulationsCopy approval review/approval for factual accuracy of promotional and informative material through VeevaEnsure all promotional material adheres to both the ABPI Code of Practice and the Medicines Act IPHAReviewing/approving promotional and informational material in line with approved product labellingTo be considered for the role of Senior Medical Information Manager, you will: Educated to degree level in a relevant scientific field Minimum of 3 years industry experience Experience in handling 2nd line MI enquiries and generating standard responses Ability to understand technical, scientific, and medical information Experience of working in Neurology and/or immunology preferred Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    • maidenhead, berkshire
    • temporary
    • full-time
    JOB TITLE:Regulatory Affairs Specialist DURATION: 12 Month contract LOCATION: Maidenhead (Can consider WFH flexibility) PAY: £40K-£45K (Dependent on experience)The ClientOn behalf of our client , who is a Global Healthcare provider , Randstad is recruiting for an individual who has a strong background in Regulatory Affairs, to sit in the role as 'Regulatory Affairs Specialist'. There are various divisions within our client- nutrition, diabetes, diagnostics- this sits within nutrition departmentThe Role Support regulatory strategy for registration and reimbursement of new products, taking into account business strategy and regulatory requirements.Ensure maintenance of in-line products.Monitor and implement new regulations to support business maintenance and growth. Support assessment of impact of upcoming regulations in the clients products to use for external engagement through Trade Associations.ResponsibilitiesProduct registration, and reimbursement, launch and maintenance. Support product registration and approval (assessment of formulas, advice on product category, handling tactics and submission timing, verification of label claims, setting mitigation plans, etc.) Negotiate with regulatory authorities during the review process to ensure registration and reimbursement approval. Effectively participate in project teams and ensure timely completion of tasks and clear communication of regulatory risks and opportunities. Ensure implementation of new regulations/guidance within legal deadlines. Approval of labels, datasheets, advertising and promo materials ensuring alignment with local regulations, Codes of Conduct, SOPs,etc. Provides technical and regulatory support to internal stakeholders. Assess and communicate impact of relevant regional regulations/standards in the local market. Administer /meet regulatory requirements to achieve excellent compliance status with no enforcement actions. Must assure that all deadlines are met. The CandidateIndividuals are able to work independently. Completed work is reviewed from a relatively long- term perspective for desired results. Individual is recognized as an industry expert and resource in regulatory affairs. Provides technical leadership to relevant departments. Desired to have a Bachelor's degree (or equivalent) in science (biology, chemistry, microbiology, medical technology, pharmacy, pharmacology, etc.) Regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related areas. Excellent written English and communication skills. Highly developed project management skills.Excellent problem solving skills. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    JOB TITLE:Regulatory Affairs Specialist DURATION: 12 Month contract LOCATION: Maidenhead (Can consider WFH flexibility) PAY: £40K-£45K (Dependent on experience)The ClientOn behalf of our client , who is a Global Healthcare provider , Randstad is recruiting for an individual who has a strong background in Regulatory Affairs, to sit in the role as 'Regulatory Affairs Specialist'. There are various divisions within our client- nutrition, diabetes, diagnostics- this sits within nutrition departmentThe Role Support regulatory strategy for registration and reimbursement of new products, taking into account business strategy and regulatory requirements.Ensure maintenance of in-line products.Monitor and implement new regulations to support business maintenance and growth. Support assessment of impact of upcoming regulations in the clients products to use for external engagement through Trade Associations.ResponsibilitiesProduct registration, and reimbursement, launch and maintenance. Support product registration and approval (assessment of formulas, advice on product category, handling tactics and submission timing, verification of label claims, setting mitigation plans, etc.) Negotiate with regulatory authorities during the review process to ensure registration and reimbursement approval. Effectively participate in project teams and ensure timely completion of tasks and clear communication of regulatory risks and opportunities. Ensure implementation of new regulations/guidance within legal deadlines. Approval of labels, datasheets, advertising and promo materials ensuring alignment with local regulations, Codes of Conduct, SOPs,etc. Provides technical and regulatory support to internal stakeholders. Assess and communicate impact of relevant regional regulations/standards in the local market. Administer /meet regulatory requirements to achieve excellent compliance status with no enforcement actions. Must assure that all deadlines are met. The CandidateIndividuals are able to work independently. Completed work is reviewed from a relatively long- term perspective for desired results. Individual is recognized as an industry expert and resource in regulatory affairs. Provides technical leadership to relevant departments. Desired to have a Bachelor's degree (or equivalent) in science (biology, chemistry, microbiology, medical technology, pharmacy, pharmacology, etc.) Regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related areas. Excellent written English and communication skills. Highly developed project management skills.Excellent problem solving skills. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
    • maidenhead, berkshire
    • contract
    • £50.00 - £62.00, per hour, Depending on experience
    • full-time
    My client, a leading pharma Biotech has an exciting opportunity for an experienced Regulatory Affairs manager to join their Asia focused Regulatory development team.As Senior RA Manager, you will:Lead regulatory strategy development for R&D portfolios and marketed products LCM for assigned projectsLead CTA & NDA/BLA filings, and CDE consultation preparation activities by working with Agents/ Third Parties/ CRO, and provide supervision to CRO project responsible, to ensure timely Regulatory filings and response to HA queriesRepresent RA and provide regulatory strategy input to support successful LCM of marketed products including line extensions and variations, and provide Regulatory expertise to local product and cross-functional teamsTo be considered for the role of Senior RA Manager, you will:Educated to degree level in a related scientific fieldMore than 10 years in drug R&D field, minimum of 5-8 years regulatory affair experience in a multinational pharmaceutical companyExperience of China / EMEA regulatory Very strong strategic background, leading activities with agencies and third parties This is a 12 Month Inside IR35 PAYE Contract. Head office in Maidenhead, flexible remote working opportunity. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.
    My client, a leading pharma Biotech has an exciting opportunity for an experienced Regulatory Affairs manager to join their Asia focused Regulatory development team.As Senior RA Manager, you will:Lead regulatory strategy development for R&D portfolios and marketed products LCM for assigned projectsLead CTA & NDA/BLA filings, and CDE consultation preparation activities by working with Agents/ Third Parties/ CRO, and provide supervision to CRO project responsible, to ensure timely Regulatory filings and response to HA queriesRepresent RA and provide regulatory strategy input to support successful LCM of marketed products including line extensions and variations, and provide Regulatory expertise to local product and cross-functional teamsTo be considered for the role of Senior RA Manager, you will:Educated to degree level in a related scientific fieldMore than 10 years in drug R&D field, minimum of 5-8 years regulatory affair experience in a multinational pharmaceutical companyExperience of China / EMEA regulatory Very strong strategic background, leading activities with agencies and third parties This is a 12 Month Inside IR35 PAYE Contract. Head office in Maidenhead, flexible remote working opportunity. Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.Candidates must be eligible to live and work in the UK.For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.

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