Working for 2 Bridge

2 Bridge is looking to strengthen its team with the following profiles:

At 2 Bridge we have a mission “together for another life”.

“Together”

alludes the concept: ‘Together Everyone Achieves More. The strength of our TEAM is extremely important for us. As a multidisciplinary team, we actively engage to ‘bridge’ different disciplines with the aim to ultimately reach a more streamlined and efficient outcome for our clients. We work closely together as a team and always strive to have an open and pleasant working relation with our clients as well as our colleagues.

“for another life”

involves on one hand our ambition to improve the lives of patients by supporting efficient and quality driven development of life science products. On the other, we also want to promote ‘another working life’ for our own 2 Bridge team members, by endorsing a healthy work/life balance.
In addition, we strongly believe in the value of talents and strive to implement those talents in our work to make a happy and effective team.

We are always on the look-out for new talent, also freelancers. If you want to join our growing team, please contact us via info@2bridge.be.

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                          CMC PROJECT MANAGER/DIRECTOR EARLY DEVELOPMENT

 

2 Bridge is a Belgian-based service provider in life sciences, that provides advice and support on all key disciplines in drug discovery, pre-clinical, clinical and product development, registration and life-cycle management.

2 Bridge works as a dynamic and adaptable team that has a wide and multidisciplinary expertise in healthcare development. We can give individual support or can operate as a ‘Tiger team’ to address complex and dynamic tasks during drug development.

Job description

We are looking for a CM&C project manager/director with experience in early development of small and/or large molecules to strengthen the CM&C team of 2 Bridge. Projects within this group can vary but usually fall within the following scope:

  • Experience with chemical/biological process development and/or formulation development.
  • Experience in physico-chemical analysis of biologicals/chemicals and knowledge of different analytical techniques used for release and stability testing.
  • Management/Leading of early development CM&C projects in multidisciplinary drug development teams.
  • Identification, selection and management of C(D)Mos
  • Preparation of Scientific, Technical and Regulatory documentation within the area of CM&C.

Desired profile

MSc/PhD in Bio-medical sciences, Bio-engineering, Biology, Industrial Pharmacy, Chemistry, or equivalent.

Manager profile: Ideally 3-5 years of experience within CM&C product development, registration and/or within a GMP production environment of large/small molecules.

Director profile: at least 10 years’ experience within CM&C drug development, registration or GMP production.

Knowledge and/or interest in pharmaceutical legislation (ICH/GMP,…).

Team-player with the ability to work independently.
Analytical, pro-active, flexible and with an eye for detail.

Interest in the overall process of health care development is a must.

Interested in working in a multidisciplinary team.
Enthusiasm with a keen interest to learn new things.
Good communication skills.
Fluency in English (especially in writing) is a must.

Do you have what it takes?

We offer an exciting job in a dynamic environment with a competitive remuneration package.

Interested? Please send your motivation letter and CV to info@2bridge.be or fill in the contact form on our website, www.2bridge.be.

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                                            TRIAL PHYSICIAN

 

 2 Bridge is a Belgian based service provider that provides scientific support, project leadership and due diligence services for pharmaceutical and health product development, registration and production.

 At the moment, we are looking for a Trial Physician to strengthen the Medical Team of 2 Bridge.

Projects within this group can vary, but the role of a Trial Physician is usually focused on leading and managing the medical activities related to a clinical study with internal and external partners.

Main Responsibilities:

  • Medical/Scientific input in clinical trial protocol: design, in- and exclusion criteria, safety follow-up, input in medical indication (SOC, guidelines, treatment), input on effect size, patient population;
  • Evaluate eligibility of patients/subjects;
  • Follow-up on adverse events, serious adverse events during trial execution;
  • Deliberation with Investigators, EC, HA, KOL;
  • Input is dose-escalation meetings/data review committees;
  • Review of medical reports, CIOMS;
  • Input in and review of Clinical Study Report;
  • Input and/or review on clinical procedural documents and processes.

Desired Profile:

  • Medical Doctor;
  • Minimum of 5 years of experience in clinical research within the pharmaceutical industry and/or CRO;
  • Team-player with strong communication and motivational skills;
  • Analytical, pro-active, flexible with an eye for detail;
  • Ability to work independently;
  • Fluency in Dutch and English is a must.

We offer an exciting job in a dynamic environment with a competitive remuneration package.

Interested? Then please send your motivation letter and CV to info@2bridge.be or fill in the contact form on our website, www.2bridge.be.

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                                             CLINICAL PROGRAM LEADER

 

2 Bridge is a Belgian-based service provider in life sciences that aims to connect the right dots across the healthcare spectrum and to provide full coverage for the key disciplines in drug discovery, development and production. 2 Bridge works as a dynamic and adaptable team that has a wide and multidisciplinary expertise in healthcare development. We give individual support or we operate as a Tiger team to address complex and dynamic tasks and to efficiently achieve our goals by combining the strengths and knowledge of our team members.

Job description

We are looking for a Clinical Program Leader to strengthen the Clinical Team of 2 Bridge which will have following main responsibilities:

  • (Co)-Leading and managing a cross-functional Clinical Team overlooking the development plan of a compound;
  • Program and Strategic Planning: leading and managing the generation of the clinical development plan in collaboration with R&D functions (Medical leader, PK expert, etc.);
  • Operations Management and Leadership: oversight of planning and execution of all clinical trials within a development program according to established timelines and budget;
  • Program timeline, resource and budget management;
  • Facilitation of issue identification and resolution, contingency planning and decision-making;
  • Contributing to the planning and preparation of clinical documents required for Health Authority interactions/submissions;
  • Development / improvement of clinical procedural documents and processes.

Desired Profile:

  • MSc in Industrial Pharmacy, Chemistry, Bio-engineering, Bio-Medical Sciences or equivalent;
  • Minimum of 7 years of project management experience in clinical research within the pharmaceutical industry and/or CRO;
  • Experience with Phase 1-3 trials as well as a working knowledge of drug development is required;
  • Team-player with strong organizational, communication and motivational skills;
  • Analytical, pro-active, flexible with an eye for detail;
  • Ability to work independently;
  • Fluency in English is a must.

Do you have what it takes?

We offer an exciting job in a dynamic environment with a competitive remuneration package.

Interested? Please send your motivation letter and CV to info@2bridge.be or fill in the contact form on our website, www.2bridge.be.

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                      COMPOUND DEVELOPMENT TEAMLEADERS (2) 

 

We are currently looking for 2 Compound Development Team Leaders to join our team.

The Compound Development Team Leader provides leadership to cross-functional teams during development of new medicines.

  • Develops and actively contributes to the strategy and execution of life-sciences development projects;
  • Builds, supports and- where needed – mentors team members, and demonstrates leadership by effective decision making;
  • Identifies potential issues and leads contingency planning and problem-solving by applying appropriate tools and techniques;
  • Accountable for overall budget and project plan deliverables;
  • Active participation in business development activities may be requested.

Desired profile

  • Advanced Degree in Health Sciences (Ph.D.), with equivalent work experience;
  • At least 10 years of professional experience with a minimum of 7 years in pharmaceutical R&D;
  • Experience in more than one key domain of R&D (Pre-clinical development, Discovery, Chemical/Pharmaceutical development, Regulatory, Clinical Development, Medical Affairs or Project Management) is essential.
  • Experience in a leadership role within a R&D organization is highly desirable.
  • Experience in multiple disease areas is highly desirable.
  • A problem solver with influencing skills and the ability to resolve conflicts in a diplomatic manner.
  • Strategic thinker with open mindset
  • Good oral/written communication skills, allowing effective interactions
  • Ability to interpret, analyse and translate interdisciplinary information.
  • Thorough knowledge of the drug development process is essential.

Do you have what it takes?

We offer an exciting job in a dynamic environment with a competitive remuneration package.

Interested? Please send your motivation letter and CV to info@2bridge.be or fill in the contact form on our contact page.