Open positions

Would you like to join and contribute to an award-winning, successful and growing multi-cultural organization in the heart of Europe and a world-leading region of the pharmaceutical industry? SFL Group and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from vibrant start-ups to established top 10 pharma and medtech companies. We have an opening for a Director / Senior Regulatory Affairs Manager Pharma The SFL regulatory team provide strategic regulatory advice and hands-on operational support for drugs, biologics and advanced therapy medicinal products (ATMPs) including gene therapy products as well as medical devices and combination products. Our experience covers all life cycle stages from development to registration and post-marketing activities. Core responsibilities

  • Leading regulatory activities on assigned projects
  • Develop and lead regulatory strategy
  • Ensuring regulatory compliance of assigned projects
  • Independent preparation of regulatory dossiers
  • Interactions with Health Authorities
  • Interactions with client contact persons
  • Coaching junior team members

Qualifications and requirements

  • Master/PhD in Pharmacy, Life Sciences or equivalent
  • Minimum of 5 years regulatory affairs experience in in consulting or pharmaceutical industry
  • Hands-on experience and sound understanding of the regulatory processes
  • Analytical and systematic thinking, organization, business orientation and flexibility
  • Experience with early development projects, including PIPs, ODDs, authority meetings and MAAs under the centralized procedure
  • Global regulatory experience is a plus
  • Able to work independently and on own responsibility under pressure
  • A highly motivated and open minded personality, able to work in an international environment
  • Excellent communication skills
  • Fluent in English; additional languages welcome

SFL offers

  • A stimulating role in an award winning company (Great Place To Work)
  • Active contribution to registration of innovative products
  • Continuous development and external educational trainings for each team member
  • Work in an energetic, motivated team
  • Rewards for outstanding accomplishments

About SFL We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU. We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU. Our main areas of expertise are Regulatory Affairs, Medical Affairs, Quality Assurance & Supply Chain, Market Access, Public Affairs, Pharmacovigilance, and Legal & Compliance. Expertise, innovation, development, respect and ethical behavior are our values and corner stones of our company culture and key to our success and excellent reputation. We are a rewarding company with an excellent environment to grow. Please send your application with CV, motivation letter and references only via email to hr_sfl@sfl-services.com (no paper applications or phone calls).

Would you like to join and contribute to an award-winning, successful and growing multi-cultural organization in the heart of Europe and a world-leading region of the pharmaceutical industry?

SFL Group and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from vibrant start-ups to established top 10 pharma and medtech companies.

We have an opening for a Regulatory Affairs Manager Pharma – Switzerland

The SFL regulatory team provide strategic regulatory advice and hands-on operational support for drugs, biologics and advanced therapy medicinal products (ATMPs) including gene therapy products as well as medical devices and combination products. Our experience covers all life cycle stages from development to registration and post-marketing activities.

Core responsibilities

  • Leading Swiss regulatory activities on assigned projects
  • Develop and lead Swiss regulatory strategy
  • Ensuring regulatory compliance of assigned projects
  • Independent preparation of Swiss regulatory dossiers
  • Interactions with Swissmedic
  • Interactions with client contact persons

Qualifications and requirements

  • Master/PhD in Pharmacy, Life Sciences or equivalent
  • Minimum of 2-3 years Swiss regulatory affairs experience
  • Hands-on experience and sound understanding of the Swiss regulatory processes
  • Analytical and systematic thinking, organization, business orientation and flexibility
  • Able to work independently and on own responsibility under pressure
  • A highly motivated and open minded personality, able to work in an international environment
  • Excellent written and verbal communication skills in both German and English

SFL offers

  • A stimulating role in an award winning company (Great Place To Work)
  • Active contribution to registration of innovative products
  • Continuous development and external educational trainings for each team member
  • Work in an energetic, motivated team
  • Rewards for outstanding accomplishments

About SFL

We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU.

We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU. Our main areas of expertise are Regulatory Affairs, Medical Affairs, Quality Assurance & Supply Chain, Market Access, Public Affairs, Pharmacovigilance, and Legal & Compliance.

Expertise, innovation, development, respect and ethical behavior are our values and corner stones of our company culture and key to our success and excellent reputation. We are a rewarding company with an excellent environment to grow.

Please send your application with CV, motivation letter and references only via email to hr_sfl@sfl-services.com (no paper applications or phone calls).

Would you like to join and contribute to an award-winning, successful and growing multi-cultural organization in the heart of Europe and a world-leading region of the pharmaceutical industry?

SFL Group and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from vibrant start-ups to established top 10 pharma and medtech companies.

We have an opening for a Director / Senior Manager Pharmacovigilance located in Switzerland or EU

Core responsibilities

  • Provide strategic input into saftey aspects of assigned product(s)
  • Lead pharmacovigilance processes and product safety reviews
  • Work closely with clients to ensure proper collection of AE case reports and reconciliation of collected data as required
  • To report Suspected Unexpected Serious Adverse Reactions to Health Authorities, ECs and investigators
  • Review of individual case safety reports according to SOPs and guidelines
  • Safety review of aggregate safety data including signal detection
  • To perform electronic reporting to Health Authority via Eudravigilance and the local authorities
  • Timely preparation of periodic reports and review of safety reports
  • Assist with internal and external drug safety audits
  • Remediate any pharmacovigilance deficiencies found during regulatory or internal audits

Qualifications and requirements

  • Bachelor/Master/PhD in Pharmacy or in Life Sciences
  • 4 years plus experience in pharmacovigilance
  • Knowledge of ICH guidelines and European safety regulations
  • A highly motivated and open-minded personality, able to work in an international team
  • Excellent organisational and problem solving skills
  • Excellent communication skills
  • Excellent skills in English is a must (verbal and writing), additional languages welcome

SFL offers

  • A stimulating role in an award winning company (Great Place To Work)
  • Work in an international, energetic, motivated team
  • Continuous development and training opportunities
  • Office- or home-based working
  • Rewards for outstanding accomplishments

About SFL

We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU.

We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU. Our main areas of expertise are Regulatory Affairs, Medical Affairs, Quality Assurance & Supply Chain, Market Access, Public Affairs, Pharmacovigilance, and Legal & Compliance.

Expertise, innovation, development, respect and ethical behavior are our values and corner stones of our company culture and key to our success and excellent reputation. We are a rewarding company with an excellent environment to grow.

Please send your application with CV, motivation letter and references only via email to hr_sfl@sfl-services.com (no paper applications or phone calls).

Would you like to join and contribute to an award-winning, successful and growing multi-national organization in the heart of Europe and one of the world’s leading regions of the pharmaceutical industry?

SFL, a Veristat company, and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from vibrant start-ups to established top 10 pharma and medtech companies.

We have an opening for a Director Biostatistic located in Switzerland or EU or the UK.

Core responsibilities

  • Direct management of Biostatistics managers and indirect management of all Biostatistics staff, including personnel development, growth, training, and leading department meetings
  • Responsible for department financials
  • Resourcing and project staffing, interviewing, hiring, and handling personnel issues
  • Lead and/or participate in corporate compliance activities as it relates to biostatistics, including development and review of department policies, SOPs
  • Ensure that Biostatistics project responsibilities are completed accurately and timely
  • Contribute to the continuous improvement of the department
  • Stay abreast of latest developments in the field of statistics in drug development
  • Collaborate with all other department functional heads, including statistical consulting
  • Attend meetings with scientific advisory groups and regulatory bodies, as needed, to support statistical aspects of regulatory submissions on behalf of sponsors
  • Provide statistical consultation on issues related to the design, analysis, and interpretation of clinical trials in a variety of therapeutic areas
  • Plan, coordinate, and provide statistical analyses, summaries, and reports of studies in the support of product development including IND/NDA and BLA submissions

Qualifications and requirements

  • PhD or Masters in Statistics, Biostatistics, math-related discipline, with applied statistics training, with 10 (ten) years of relevant work experience
  • Minimum of 5 years of experience in personnel management
  • Thorough knowledge of ICH, GCP guidelines and other applicable regulatory rules
  • Demonstrated ability to lead by example, and demonstrated skill for technical and supervisory leadership of staff
  • Excellent written and oral communication skills including grammatical/technical writing skills
  • Excellent interpersonal, communication, and organizational skills with the ability to work independently as well as in a team environment
  • Experience with regulatory agencies, such as the FDA or EMA
  • Skilled in use of computer technology, including SAS, and ability to learn new applications

SFL offers

  • A stimulating role in an award winning company (Great Place To Work)
  • Active contribution to registration of innovative products
  • Continuous development and external educational trainings for each team member
  • Work in an energetic, motivated team
  • Rewards for outstanding accomplishments

About SFL

We provide innovative and customized services and solutions in the life science field from offices in Switzerland, EU and the UK.

Expertise, innovation, development, respect and ethical behavior are our values and corner stones of our company culture and key to our success and excellent reputation. We are a rewarding company with an excellent environment to grow.

Please send your application with CV, motivation letter and references only via email to hr_sfl@sfl-services.com (no paper applications or phone calls).

Would you like to join and contribute to an award-winning, successful and growing multi-national organization in the heart of Europe and one of the world’s leading regions of the pharmaceutical industry?

SFL, a Veristat company, and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from vibrant start-ups to established top 10 pharma and medtech companies.

We have an opening for a Senior Biostatistician located in Switzerland or EU or the UK.

Core responsibilities

  • Analyzes clinical trial data producing accurate results representing the outcome of the trial, validates statistical output, accurately interprets and clearly communicates statistical results and concepts to non-statisticians.
  • With the medical writer, co-authors final integrated reports of clinical trial data by writing thorough and clear statistical methods sections and producing the statistical appendix.
  • Provides statistical output as required for manuscripts and ensure that the results are accurately interpreted in the publications.
  • Provides input into statistical SOPs and general standardization efforts (e.g., statistical methodology standards, standard data presentations) and participates in interactions with regulatory agencies, as required.
  • Collaborates effectively with members of clinical trial implementation teams and with Biometrics colleagues, and keeps abreast of new developments in statistics, drug development, and regulatory guidance through literature review and attendance at workshops and professional meetings.

Qualifications and requirements

  • PhD degree in Statistics, Biostatistics, or related field, and 3 years of biostatistical experience
  • Excellent written and oral communication skills including grammatical/technical writing skills, and familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials are required.
  • Familiarity with SAS, SPSS or other statistical software package.
  • Proficiency in Microsoft Word and Excel.
  • Strong level of detail orientation.
  • Ability to work on multiple tasks under tight timelines.

SFL offers

  • A stimulating role in an award winning company (Great Place To Work)
  • Active contribution to registration of innovative products
  • Continuous development and external educational trainings for each team member
  • Work in an energetic, motivated team
  • Rewards for outstanding accomplishments

About SFL

We provide innovative and customized services and solutions in the life science field from offices in Switzerland, EU and the UK.

Expertise, innovation, development, respect and ethical behavior are our values and corner stones of our company culture and key to our success and excellent reputation. We are a rewarding company with an excellent environment to grow.

Please send your application with CV, motivation letter and references only via email to hr_sfl@sfl-services.com (no paper applications or phone calls).

Would you like to join and contribute to an award-winning, successful and growing multi-cultural organization in the heart of Europe and a world-leading region of the pharmaceutical industry?

SFL Group and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from vibrant start-ups to established top 10 pharma and medtech companies.

In our Basel office, we have an entry position for a Public Affairs Associate.

The SFL Public Affairs & Regulatory Intelligence team has longstanding experience in supporting clients to anticipate and analyze changes in EU and Swiss healthcare policy and regulatory environment, to conduct stakeholder mapping and to plan and adapt engagement strategies with stakeholders relevant for their portfolios and corporate positions. Our high-quality global intelligence, materials and strategic advice is tailored to our clients’ specific needs. We do provide association management and communicate the members’ views with key stakeholders.

In our Basel office, we have an opening for a Public Affairs Associate. The position provides an opportunity to work in Public Affairs at the forefront of the healthcare sector in a multinational, multi-disciplinary environment. The working language for the internship is both German and English.

Core responsibilities

  • Support the Public Affairs team on a project by project basis
  • Providing support with the management of associations
  • Assisting in organizing conferences as well as workshops for SFL and our clients
  • Development of communication materials (newsletter, press releases, brochures, leaflets, slide decks)
  • Management of online communication activities
  • Support screening and analysis of draft laws, policies and regulatory guidance that are relevant for the life sciences sector
  • Provide ad-hoc support to other functions at SFL, as necessary

Qualifications and requirements

  • Bachelor or master in communication, life sciences, political sciences, journalism, or other relevant field
  • Minimum of 2 years work experience in public affairs, communication, or other relevant field
  • Good knowledge of Swiss as well as EU health policy
  • Excellent writing and verbal skills in both German and English
  • Good knowledge of social media and website management and editing
  • Previous experience in communications/events/public relations is desirable
  • Good working knowledge of Microsoft Office
  • Experience in project management is an asset
  • Organized but flexible and open-minded personality with keen interest to learn
  • Able to work independently and on own responsibility under pressure
  • Strong interest in pharmaceutical and medtech industry

SFL offers

  • A stimulating role in an award winning company (Great Place To Work)
  • Active contribution to registration of innovative products
  • Continuous development and external educational trainings for each team member
  • Work in an energetic, motivated team
  • Rewards for outstanding accomplishments

About SFL

We provide innovative and customized services and solutions in the life science field from offices in Switzerland and the EU. Our main areas of expertise are Regulatory Affairs, Medical Affairs, Quality Assurance & Supply Chain, Market Access, Public Affairs & Regulatory Intelligence, Pharmacovigilance, and Legal & Healthcare Compliance.

Expertise, innovation, development, respect and ethical behavior are our values and corner stones of our company culture and key to our success and excellent reputation. We are a rewarding company with an excellent environment to grow.

Please send your application with CV, motivation letter and references only via email to hr_sfl@sfl-services.com (no paper applications or phone calls).

NOTICE TO SEARCH FIRMS/THIRD PARTY RECRUITMENT AGENCIES (RECRUITERS)

The Human Resources team manages the recruitment and employment process for SFL. Unsolicited resumes sent to SFL from recruiters do not constitute any type of relationship between the recruiter and SFL and do not obligate SFL to pay fees should we hire from those resumes. Recruiters are requested not to contact or present candidates directly to our hiring managers or employees.