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Life Science Specialists

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VIEW OUR SPECIALISMS

TESTIMONIALS

  • “I had the pleasure of working with Hamlyn Williams on a very tough search. They are consummate professionals, a reliable and knowledgeable recruiter.  Being very responsive, they took the time to understand the requirements of the position and asking the right questions. They were adaptable, continuously finetuning the search, and was very thorough in their screening process. They continued to recruit for the position even after the right candidate had been identified, and up to the point where an offer was extended, something very few agency recruiters tend to do. They are among my most dependable recruitment partners, and I would enjoy the opportunity to work with them again.”

    Kavitha Manley
    Kavitha Manley

    Associate Director, Talent Acquisition

WE ARE GLOBAL


WE CAN SUPPORT YOUR BUSINESS AS IT GROWS

We operate globally with 7 offices across the EMEA, N.America and APAC regions.

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RESEARCH & DEVELOPMENT

HW Life Sciences places leading professionals within the Biotech, Pharmaceutical, Medical Device and Medical technology industries at the research  and development phase of the life cycle.

PRODUCTION

HW Life Sciences places industry leading professionals within Biotech, Pharmaceutical, Medical Device and Medical Technology industries at the production phase of the development life cycle.

COMMERCIALIZATION

HW Life Sciences places industry leading professionals within Biotech, Pharmaceutical, Medical Device and Medical Technology industries post product approval to commercialization. 

OUR LATEST JOBS


  • Financial Services and Banking

  • Life Sciences

  • Technology
  • BSA Risk Assessment/Policy Writing FVP

    REMOTE

    A banking client in Los Angeles is looking for an experienced BSA professional who has focused on both Risk Assessments and Policy writing. This individual will be responsible for BSA/OFAC Program Office policy and advisory work including; policy research and analysis, drafting policy program documentation in coordination with both 1st and 2nd LODs. Working as part of a 5 person team, you MUST be able to work both independently and also as part of a cohesive unit! Responsibilities: Reviewing and copy-editing policy, program and procedural documentation Advising internal clients regarding internal policy, program and procedural matters Risk Assessment and Methodology Documentation Responsible for all activities related to periodic update, including drafting and version control activities, of BSA/OFAC risk assessment processes Assisting the Deputy BSA Officer with management participation in the Bank’s New Product and Services process Responsible for coordinating and regular updates to Management Actions Plans Requirements: Bachelor’s Degree and CAMS certification (ideally) 5-8 years’ worth of banking experience in a BSA role 3+ years’ worth of policy writing and risk assessment experience, either in an in-house or advisory capacity THIS IS A REMOTE ROLE, BUT WILL REQUIRE SOMEONE TO BE LOCATED IN ONE OF THE AREAS THAT THIS BANK HAS A FOOTPRINT (CA, WA, TX, IL, NY, GA). If this opportunity interests you, please contact the team today: sd-compliance@hamlynwilliams.com.

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  • Operations & Strategy Head

    REMOTE

    A Fintech client is looking for a Payments expert to lead its Strategy and support the company’s Operational functions. This is a senior level role that will have visibility across multiple business lines, mainly the Sales teams. Main responsibilities:  Design, plan and implement business strategies, plans and procedures  Set comprehensive goals for business growth and success by identifying new business and generating new opportunities Possess a strong understanding of strategic planning and team leadership, leveraging on technology to enable growth and optimize the business  Experience working with Board of Directors and internal stakeholders to keep regular updates on business performance and progress Requirements: Bachelor’s degree 8+ years of experience leading at a fast-growing startup company An understanding of the payments industry is crucial If this opportunity interest you, please get in touch!

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  • Credit Specialist - VP

    Bay Area

    We are partnered with a banking client in the Bay Area that is looking for an experienced VP level Credit Specialist to develop process for monitoring small business and consumer credit card portfolios, as well as a process for delinquency management of these portfolios. Joining the team in a REMOTE capacity, this person would provide guidance on development of underwriting scorecards for businesses and criteria for automated credit decisions. Working alongside the treasury head of consumer products, the key goal is to design controls and processes to minimize credit and fraud losses and maintain compliance with bank and regulatory requirements.  As a Senior VP Credit Specialist, you will: Credit Monitoring Establish programs and reporting for credit monitoring of business and consumer credit portfolios. Work closely with Commercial Banking portfolio management team on processes for recommending increases, decreases or holds on business card lines. Implement programs for consumer cards for determining when cardholders are eligible for line increases, decreases or holds. Delinquency Management Acts on past due accounts in accordance with Bank policy and procedure to ensure the collectability of such accounts. This may require working with the Commercial Portfolio Management team or with our Consumer Loan Collections area. Establish collections program using our processor, FIS, ss the portfolio grows and 2orks with in-house legal on procedures related to bankruptcies. Underwriting Provide support to underwriting business and consumer credit cards by developing criteria for automated credit decisioning. Research and recommend risk-management tools and products to incorporate into automated decisioning for business and consumer cards. Assists with risk-based pricing of consumer card products. As a Senior VP Credit Specialist, you will need: Bachelor's degree in related field and 3+ years’ experience in a Commercial Bank loan credit function Broad knowledge of credit related to business and consumer cards with understanding and experience in credit card underwriting, credit monitoring and delinquency management. Familiarity with tools available through companies such as Experian or Plaid Current knowledge of federal and state laws related to credit card lines and bankruptcy laws. If you are a skilled Credit Specialist, you can apply by: Selecting the “Apply” button below or by contacting me directly. As a Compliance & Financial Crime market specialist, I am partnered with a myriad of large and small Financial Services and Banking Institutions across the West Coast. If this role is of interest to you, or if you are interested in exploring other opportunities within the market, you are welcome to reach out directly to: Christian Bohn, c.bohn@hamlynwilliams.com or (619) 350 – 6348  

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  • Automation Lead - Quality Engineering

    Hong Kong

    My client is a globally renowned consultancy operating international and local business lines to integrate the best technology available into Financial Services. They have been continuously growing throughout 2020 and the software engineering team is now looking for a hands-on Automation QA Lead to spearhead and deliver on various upcoming digital initiatives.    Requirements:   5+ years of experience in leading automation teams.    Programming experience in Java or Python with hands on experience using Selenium, Appium,  Robot Framework, TestNG, TDD/BDD Experience with financial services domain highly regarded Experience in AGILE and CI/CD best practices Great communication skills, fluent Cantonese and/or English 

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  • Senior Director Regulatory Affairs Advertising & Promotion

    San Diego, California

    Director Regulatory Affairs, Advertising & Promotion Location: San Diego, California Type: Full Time Permanent Salary: Excellent salary, bonus and accompanying benefits package. Remote Consideration. Excellent opportunity to spearhead and own the Advertising/Promotion function with my client as they look to move to commercialization with their leading oncology candidate. Excellent clinical company with an incredible pipeline and amazing financial stability! SCOPE: This person will be the direct lead for the reviewing and approving of all promotional/non promotional materials for products to ensure compliance with FDA regulations and guidelines. This position requires an ability to understand and evaluate all perspectives of promotions and advertising and provide clear regulatory guidance.  RESPONSIBILITIES: Internal expert on global regs (FDA, EMA, PMDA etc) and guidance on trends governing the promotion of pharmaceutical products Understand and evaluate all perspectives of promotions and advertising while providing clear regulatory guidance Act as primary contact with FDA’s Office of Prescription Drug Promotion Lead and manage Materials Review Committee (MRC) meetings and collaborate with internal/external teams Interacting with commercial, medical, and legal teams to ensure compliance Keeping current with industry and regulatory developments relating to advertising and promotion, including interpretation of FDA enforcement letters, interpretation of new and updated Guidance Documents for Industry, and, as applicable, evaluating related internal policies/best practices and processes.    EDUCATION/EXPERIENCE: BS/BA necessary, graduate degree preferred Min of 8 years of biopharma experience, at least 5 years in Regulatory Affairs within Ad/Promo Complete Understanding of US law and regulations in related to communications about prescription drugs and investigational treatment I manage a range of other permanent and freelance positions for a broad portfolio of clients (Biotech, CRO and Pharma). If the above role isn’t for you but you’d nevertheless like to discuss your options in the market, I’d welcome a confidential discussion by phone or email. Contact Bobby DeMarco at (619) 784 9869.    

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  • Remote Senior Clinical Research Associate

    Remote (United States)

    SENIOR CLINICAL RESEARCH ASSOCIATE SCOPE Exciting opportunity to join the growing Clinical Operations team in a market-leading company with a robust clinical oncology portfolio. As Senior Clinical Research Associate, you will be responsible for the initiation and documentation of multi-site clinical trials. This company offers a competitive salary and benefits package and the opportunity for promotion and career growth.  RESPONSIBILITIES Create and maintain documentation and tracking for site initiation activities, site management, monitoring visit findings, subject screening and enrollment Participate in site intiation activities Train and oversee CRO and vendors on site activities Conduct and document pre-study, initiation, progress and closeout monitoring visits Verify subject safety and site adherence to FDA Regulations and ICH/GCP Guidelines Review CRF, Informed Consent Documents and verification of data management queries in to meet clinical study timeline Oversee vendors and CROs, including reviewing invoices and expenses REQUIREMENTS Bachelor’s degree in life sciences, biology, or related required 3+ years CRA experience in biotechnology, biopharmaceuticals or pharmaceutical company required Experience in oncology clinical trials required; experience with solid tumor indiciations strongly preferred Travel required (20-40%) My team and I are working on a number of additional opportunities for a broad portfolio of clients across the US and internationally. If this role isn't for you but you would like to explore your options in the market, I would welcome a confidential conversation at your convenience. Please contact me at (619) 350-6149 or e.mato@hamlynwilliams.com. 

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  • Remote Clinical Research Associate

    Remote (United States)

    CLINICAL RESEARCH ASSOCIATE (CRA) SCOPE Exciting opportunity to join the growing Clinical Operations team in a market-leading company with a robust clinical oncology portfolio. As Clinical Research Associate, you will be responsible for the initiation and documentation of multi-site clinical trials. With a team-oriented culture and a successful pipeline, this company is the place to continue growing in your career. RESPONSIBILITIES Create and maintain documentation and tracking for site initiation activities, site management, monitoring visit findings, subject screening and enrollment Conduct and document pre-study, initiation, progress and closeout monitoring visits Verify subject safety and site adherence to FDA Regulations and ICH/GCP Guidelines Review CRF, Informed Consent Documents and verification of data management queries in to meet clinical study timeline Oversee vendors and CROs, including reviewing invoices and expenses REQUIREMENTS Bachelor’s degree in life sciences or health care required 2+ years CRA experience in biotechnology, biopharmaceuticals or pharmaceutical company required Experience in oncology clinical trials required Monitoring experience required Strong communication and writing skills Strategic thinker with the ability to thrive in a collaborative, fast paced environment Travel required (up to 40%) My team and I are working on a number of additional opportunities for a broad portfolio of clients across the US and internationally. If this role isn't for you but you would like to explore your options in the market, I would welcome a confidential conversation at your convenience. Please contact me at (619) 350-6149 or e.mato@hamlynwilliams.com. 

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  • Senior Clinical Trial Manager

    Massachusetts

    Our client is a leading precision oncology company actively hiring for a Senior Clinical Trial Manager reporting directly into the Senior Director of Clinical Operations. The client is rapidly growing and looking for the most exceptional individual with a strong desire and eagerness to be part of an innovative team developing breakthrough cancer therapies in their MA based office. Job Description: Ability to lead cross-functional trial team to establish delivery of intricate clinical trials and manages protocol execution Oversee CROs and vendors to ensure timelines are met with efficiency, quality and within budget, and in accordance with SOPs, GCP Ability to anticipate and identify operational risks and mitigation plans within clinical trials and presents any issues needing escalation or recommends contingency plans as necessary to Head of Clinical Ops. Ensure accurate tracking and reporting of study metrics, timelines, update of trial information in all trial databases and tracking systems while establishing study milestones.   Qualifications: 5+ years experience in Clinical Trial Management specifically in a pharmaceutical/biotechnology industry with leadership experience Bachelor’s degree in health related field Oncology background is highly desirable Comprehensive understanding of the clinical trial database life cycle with an understanding of FDA/ICH guideline   Apply here or by direct contact (646) 349-2959 l.wysocki@hamlynwilliams.com if you are interested in working with an innovative and growing biotech company.

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  • C++ Senior Developer (Global candidates welcomed)

    Hong Kong

    Responsibilities Lead in designing and developing of market making and trading algorithms. Work with a diverse team of developers and with traders on improving trading strategy. Contribute to all levels of the SDLC as to develop software to support the trading operations. Help coordinate various software development efforts across the company. Collaborate with traders to understand and anticipate trading technologies needed. Document software performance and proactively optimize as needed.   Requirements 5+ years working experience in algorithmic trading environment and/or high frequency trading system development. Proficiency in C++11/14/17. Experience in Java/Scala/C#/Rust/Python would be a plus. Experience in Memory/CPU profiling/optimization, multi-threading and distributed computing. Experience in using high performance messaging bus such as ZMQ, RabbitMQ, ActiveMQ. Experience in developing on the Linux platform with libraries such as BOOST and STL. Experience with revision control tools such as Git.

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  • Automation Lead - Quality Engineering

    Hong Kong

    My client is a globally renowned consultancy operating international and local business lines to integrate the best technology available into Financial Services. They have been continuously growing throughout 2020 and the software engineering team is now looking for a hands-on Automation QA Lead to spearhead and deliver on various upcoming digital initiatives.    Requirements:   5+ years of experience in leading automation teams.    Programming experience in Java or Python with hands on experience using Selenium, Appium,  Robot Framework, TestNG, TDD/BDD Experience with financial services domain highly regarded Experience in AGILE and CI/CD best practices Great communication skills, fluent Cantonese and/or English 

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  • Senior FI CO Central Finance Consultant

    Remote / Switzerland

    We are partnered with one of the Big 4 in Switzerland and due to extensive growth of their consultancy business are looking for a German speaking for a Senior SAP FI CO Central Finance Consultant to join their team to work on exciting S/4 Hana transformation projects. We would also be interested in speaking with junior and management consultants. As a Senior FI CO Central Finance Consultant You Will: Work on hot topics such as S/4 Hana Work with the client side supporting the full life cycle Expect new challenges every day and work with numerous different industries Have a clear path for progression Flexible Working As a Senior FI CO Central Finance Consultant You Will Need: Good knowledge of business processes and experience in making recommendations for process improvements Detailed understanding of SAP S4HANA Central Finance   including transactions and configuration options More than four years’ professional experience in consulting in the area of SAP Finance and Controlling. Good understanding of the managerial and financial accounting principle. Strong analytical capabilities and communication skills You communicate confidently in English Willingness to travel, particularly in Europe when safe If this is you please select the apply button below or contact me directly, I am an SAP market specialist working with a large variety of clients across Europe in various different industries. If this role is of interest to you, or if you’d like to explore other opportunities in the market, please feel free to reach out directly. Contact Chris Day at 020 3878 4790 or at c.day@hamlynwilliams.com.

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  • Regional cyber security manager

    Hong Kong

    Reporting to IT Manager, this incumbent is responsible for building secure software, monitoring system and infrastructure at the highest security standard. He/ she will design, build and manage security solutions, perform technical security assessments and vulnerability testing to highlight and mitigate risks. He/ she will also work closely with Group and Regional IT to design and build a robust system to enhance the security of our infrastructure and systems. Responsibilities Support the region in the areas of Information & Cyber Security and Network & Infrastructure. Lead the Global Incident Management process for incidents within region and support globally if needed. Work closely with the Security Engineer lead and Global Security team to meet policy & technical standards. Support the ongoing development of the IT Security strategy that improves the security posture for our employees and data Ensure all Security Applications and Tools are implemented and managed in region. Evaluate, maintain and configure security functions within Business Applications. Ensure Vulnerability Management & Patch Management are implemented, analysed and appropriately actioned. Lead and support remediation tasks required based on Internal & External Penetration Testing. Setup and maintain network VLANs and other controls to support security segmentation. Keep abreast of all emerging technical vulnerabilities, report on them and make appropriate plans to remediate. Support the regional and global teams in ensuring that the business is compliant with Data Protection Regulation. (GDPR), CCPA, Payment Card Industry Data Security Standards (PCI-DSS) and local regulations and other standards. where applicable. Assist with the development security controls in alignment with good practice frameworks, e.g. ISO27001/2, NIST CSF, PCI-DSS. Help raise awareness and knowledge about information security and risk of cyber space through various channels and means Qualifications Degree in Computer Science/ Engineering/ Information Systems or a related discipline At least 5 years of relevant experience in information/ cyber security Hands-on experience implementing and maintaining network & infrastructure solutions Practical knowledge of Enterprise Security Applications, e.g. Carbon Black, Azure Security Center, Mimecast, Qualys etc. Excellent communication skills both written and verbal with the ability to interact effectively with senior both technical and non-technical teams, including strong experience in delivering business and systems change initiatives. Track record in analysing business requirements and delivering technical business solutions. Ability to write clear business documentation, such as business process documents, technical specifications and training documents. Ability to effectively manage multiple projects/tasks of varying complexities, meet deadlines and work well under pressure. Any Network, Infrastructure or Security related certifications are a huge plus

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JOIN THE CONVERSATION

CQV Engineers join the conversation online! Our LinkedIn group is a place for you to talk about related subjects, hot topics in the industry or a place to discuss certain problems that have arisen in your day to day work, as well as brand new job opportunities that arise.

Engineers globally are welcome!

ABOUT US

Hamlyn Williams Life Sciences was established in January 2016 to respond to the shortage of Regulatory Professionals across the Life Sciences out of our New York Office by now Director Alex McGarel.

Since then we have grown to a global team of over 20 consultants spread across our seven offices servicing the most innovative Pharmaceutical, Biotech, Medical Technology and Medical Device organizations in the hope of playing our part and providing the best talent enabling our clients to continue to innovate in the space and bring therapies to the global consumer in the fight to diagnose, treat, cure & ultimately prevent Human Disease.

Our specialist consultants work with the best talent across the Research, Regulatory, Production & Commercialization  stages of the drug development life cycle.


Our launch of Hamlyn Williams Life Sciences is an exciting step for our truly global business . If you have enquiries regarding opportunities or partnering to grow your team please reach out to our Head of US Life Sciences Alex McGarel or Head of EMEA James Brookes.

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