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Job Offers Medical
Specialist in Orthopaedics and Trauma Surgery (m/f/d), Germany, Baden-Wuerttemberg, Ref. 130
For our client, a hospital in Rhineland-Palatinate, we are looking for a:
Specialist in Orthopaedics and Trauma Surgery (m/f/d)
Reference number: 130
Location: Rhineland-Palatinate, Germany
Contract type: Full time
Area/department: Orthopaedics and Trauma Surgery
Salary: According to TVöD-K (Public Sector Collective Agreement)
Orthopaedics and trauma surgery is about more than clinical procedures; it is the craft of restoring independence and movement to people’s lives. There is a unique sense of fulfilment in seeing a patient take their first pain-free steps following your intervention. We are looking for a surgeon who combines technical precision with genuine empathy—someone who understands that behind every fracture and joint condition is a person eager to return to their daily life. If you are looking for a role where your surgical expertise is matched by a culture of mutual respect, this is the place for you.
How you will make an impact:
In this role, you will take on a key position within our surgical team, driving clinical excellence and patient care:
• Performing complex surgical procedures in general orthopaedics and trauma surgery.
• Taking full clinical responsibility for your patients, from initial diagnosis to post-operative recovery.
• Contributing your expertise to our outpatient clinics and diagnostic consultations.
• Working closely within a multidisciplinary team to ensure the highest standards of patient safety.
• Participating in the hospital’s on-call and background shifts.
• Mentoring and supervising junior doctors as they progress through their specialist training.
• Helping to shape and refine internal clinical pathways and quality management protocols.
What you bring to the role:
You combine surgical skill with a collaborative spirit and a commitment to patient-centred care:
• Fully qualified Specialist (Facharzt) in Orthopaedics and Trauma Surgery.
• Proven surgical experience and confidence in standard orthopaedic and trauma procedures.
• A strong sense of accountability and the ability to make decisive clinical judgements.
• A team-oriented mindset with a passion for sharing knowledge.
• Excellent communication skills, showing empathy to patients and their families.
• Proactive engagement in the further development of the department.
• German language proficiency (C1 Medical level) to ensure safe clinical documentation and patient interaction.
Why you will love working here:
We provide an environment where your dedication is recognised and your professional growth is a priority:
• Competitive salary based on the TVöD-K tariff, including a generous company pension scheme.
• A structured induction within a supportive, highly skilled team that values flat hierarchies.
• Extensive funding and support for your continued professional development and specialisation.
• A modern workplace equipped with the latest surgical and diagnostic technology.
• Flexible working models designed to help you maintain a healthy work-life balance.
• Assistance with relocation or finding suitable local accommodation if required.
• Located in the beautiful region of Rhineland-Palatinate, offering high quality of life and excellent connections.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Radiologist (Specialist in Radiology) (m/f/d), Germany, Bavaria, Ref. 123
Are you a Radiologist (Specialist in Radiology) (m/f/d) and looking for a new professional challenge? Then you’ve come to the right place!
For our client, a hospital in Bavaria, we are looking for:
Ref.: 123
Position: Radiologist (Specialist in Radiology)
Location: Bavaria, Germany
Employment Type: Full-time
Department: Internal Medicine
Salary: In accordance with the collective bargaining agreement
Tasks:
- Perform and interpret diagnostic imaging procedures (e.g. MRI, CT, X-ray)
- Document and report imaging findings in a detailed manner
- Collaborate closely with the Internal Medicine team in interdisciplinary case reviews
- Participate in tumor boards and clinical conferences
- Provide mentorship and supervision to junior physicians and trainees
Requirements:
- Medical license and board certification as a Radiologist
- At least 2 years of clinical experience in a hospital or radiology practice
- Proficiency with modern radiology software and PACS systems
- Strong commitment to patient care and empathetic communication
- Excellent teamwork, communication skills, and a proactive, independent work style
- Fluent in German; good English skills are an advantage
Benefits:
- Comprehensive onboarding and tailored continuing education programs
- Company pension plan and additional health services
- Flexible working hours and the option for part-time or home-office days
- Commuting allowance and subsidized staff housing opportunities
- State-of-the-art equipment in our newly established radiology center
- Regular team-building events and wellness initiatives
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Registered Nurse (m/f/d) for Intensive Care Unit, Germany, Lower Saxony, Ref. 121
Are you a Registered Nurse (m/f/d) for Intensive Care Unit and looking for a new professional challenge? Then you’ve come to the right place!
For our client, a hospital in Lower Saxony, we are looking for a Registered Nurse for Intensive Care Unit .
Ref.: 121
Position: Registered Nurse (m/f/d) for Intensive Care Unit
Location: Lower Saxony, Germany
Contract Type: Part-time
Department: Intensive Care Unit
Salary: Collective Bargaining Agreement (Tarifvertrag)
Responsibilities:
- Monitor and care for ICU patients (e.g., ventilation management, vital sign monitoring, medication administration).
- Collaborate with physicians and nursing colleagues to adjust treatment plans continuously.
- Document nursing processes and prepare detailed care and handover reports.
- Participate in emergency response and resuscitation teams following hospital guidelines.
- Contribute to quality assurance measures and interdisciplinary patient rounds.
Requirements:
- Completed training as a registered nurse (Gesundheits- und Krankenpfleger) or equivalent qualification.
- Several years of professional experience, ideally in an intensive care setting.
- Valid certifications in life-saving emergency procedures (e.g., BLS, ACLS).
- Proficient in German (spoken and written; at least C1 level).
- Strong teamwork skills, excellent communication, and high commitment.
- Resilience, sense of responsibility, and an organized approach to work.
Benefits:
- Comprehensive onboarding and regular training opportunities (e.g., specialized ICU courses).
- Company pension plan and capital-forming benefits.
- Flexible scheduling with shift-swapping options and various part-time arrangements.
- Subsidized public transportation or discounted parking.
- Health promotion programs (e.g., workplace fitness, back care courses).
- Regular team-building events and a friendly work environment.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Specialist in Neurology (m/f/d), Germany, Bavaria, Ref. 120
Are you a specialist (m/f/d) in neurology and looking for a new professional challenge?
Then you’ve come to the right place!
For our client, a hospital in Bavaria, we are looking for a Specialist in Neurology.
Ref.: 120
Position: Specialist in Neurology (m/f/d)
Location: Bavaria, Germany
Contract Type: Full-time
Department: Neurology
Salary: Collective Bargaining Agreement (Tarifvertrag)
Responsibilities:
- Diagnose and treat a wide range of neurological disorders in both inpatient and outpatient settings
- Perform and interpret EEG and EMG examinations
- Provide comprehensive patient care, including consultations and follow-up
- Collaborate closely with interdisciplinary teams (e.g., Neuroradiology, Neurosurgery, Rehabilitation)
- Supervise and mentor junior doctors and participate in clinical case conferences
Requirements:
- Medical license (Approbation) in Germany
- Board certification in Neurology or in the final stage of training
- Several years of hands-on experience in clinical neurology
- Proficiency in EEG, EMG, and neurosonology diagnostics
- Fluent German (C1 level or higher); English skills are an asset
- Strong team orientation, empathy, and excellent communication skills
- Self-driven work style, high sense of responsibility, and dedication
Benefits:
- Competitive salary in accordance with the current TV-Ärzte/VKA or TVöD, including premium payments
- Company pension plan and capital-forming benefits
- Extensive opportunities for continuing education and professional development (e.g., specialist courses, conference attendance)
- Flexible working hours with flextime arrangements and on-call schedules by mutual agreement
- Childcare subsidy and support for work–life balance
- Public transport allowance or company car options
- Regular team-building events and a supportive, modern work environment
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Resident Physician (m/f/d), Internal Medicine, Germany, Rhineland-Palatinate, Ref. 119
Are you a resident physician (m/f/d) in internal medicine looking for a new professional challenge?
Then you’ve come to the right place!
For our client, hospital in Rhineland-Palatinate, we are looking for a resident physician in internal medicine.
Ref.: 119
Position: Resident Physician – Internal Medicine
Location: Rhineland-Palatinate, Germany
Contract Type: Full-time / Part-time
Department: Internal Medicine
Salary: Not disclosed
Your responsibilities:
- Clinical care for patients with internal medicine conditions in the ER and on the ward
- Conducting medical history interviews, clinical exams, and contributing to diagnostics
- Assisting in the creation and execution of treatment plans Involvement in emergency care and acute internal medicine procedures
- Documentation of findings and treatment progress
- Participation in diagnostic and therapeutic interventions
Your profile:
- Valid medical license from Germany or an EU member state
- Currently training to become a board-certified internal medicine specialist
- Strong sense of responsibility, communication skills, and teamwork
- Resilience, independence, and empathy towards patients
- Willingness to work in interdisciplinary settings
Benefits:
- Full training authorization in internal medicine, cardiology, gastroenterology, and angiology
- Opportunity to earn additional emergency medicine qualification (costs fully covered)
- Company pension plan
- Internal training and external training
- Flexible working models for family/work-life balance
- Employee discount app with top offers
- Affordable housing in an attractive region
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Specialist Physician or Medical Doctor (m/f/d) for the Emergency Department, Germany, Hesse, Ref. 118
Are you a specialist physician or medical doctor (m/f/d) passionate about emergency medicine and looking for a new challenge?
Then you’ve come to the right place!
We are currently recruiting on behalf of our client – a hospital in Hesse– for a motivated doctor to join the Emergency Department.
Ref.: 118
Position: Specialist Physician / Medical Doctor (m/f/d) – Emergency Department
Location: Hesse, Germany
Contract Type: Full-time
Field: Emergency Medicine
Salary: No information
Duties:
- Initial assessment and diagnostics of emergency patients in close cooperation with senior physicians and the ED leadership
- Care and treatment of patients in the observation unit
- Contribution to the structural and organizational development of the ED
- Close collaboration with other departments, wards, ICU, and bed management
Requirements:
- Demonstrable good to very good knowledge of German (B2 or C1 certificate) or good knowledge with willingness to improve.
- Passion for emergency medicine.
- Team spirit and stress resilience.
- Willingness to work in an interdisciplinary team.
- Desire to live in Germany.
Advantages:
- Diverse workdays with modern equipment in an independent ED.
- Flat hierarchies and family-friendly duty schedules.
- 24-month additional training in clinical acute and emergency medicine.
- Opportunity to participate in emergency medical services.
- Support for further education (time and financial assistance).
- Salary according to TV-Ärzte/VKA and extensive employee benefits.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Assistant Physician, Internal Medicine and Cardiology, Germany, Baden-Württemberg, Ref. 116
Are you a Assistant Physician, (m/f/d) for internal medicine and looking for a new professional challenge?
Then you've come to the right place!
For our client, a hospital in Baden-Württemberg, we are looking for a General Practitioner, Internal Medicine.
Ref.: 116
Position: Assistant Physician – Internal Medicine
Location: Baden-Württemberg, Germany
Contract Type: Full-time
Department: Internal Medicine
Salary: Not disclosed
Duties:
Working as an assistant physician for internal medicine in the emergency department and on interdisciplinary wards.
Completion of training in various specialities of internal medicine.
Requirements:
Passion for internal medicine.
Ability to work independently, sense of responsibility, ability to work in a team, commitment and willingness to learn.
High priority for patient safety and flexibility.
Advantages:
- Structured training programme with extensive specialist training through rotation.
- Regular assignments in functional diagnostics to fulfil the further training catalogue.
- Possibility of further training in general medicine through rotation between internal medicine and surgery clinics.
- Support in obtaining the specialist title in radiation protection and/or emergency medicine as well as other further training programmes.
- Remuneration according to the TV-Ärzte/VKA.
- Opportunities for an above-average income through compensation for on-call duties in accordance with the Working Hours Act.
- Interesting and varied area of responsibility in a collegial environment with flat hierarchies.
- Full authorisation for further training as a specialist in internal medicine as well as authorisation for further training in gastroenterology, angiology, cardiology, geriatrics and special internal intensive care medicine.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Registered Nurses (m/f/d) – Intensive Care, Germany, North Rhine-Westphalia, Ref. 114
For our German client (a hospital in North Rhine-Westphalia region) we are looking for registered nurses, intensive care.
Ref.: 114
Position: Registered nurses
Location: North Rhine-Westphalia, Germany
Type of contract: Full-time
Sector: Intersive care
Salary: Remuneration according to TVöD-K with corresponding public service benefits and various social benefits.
Job Description:
Join a multidisciplinary team committed to excellent patient care and collegial collaboration.
Your responsibilities include:
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Professional care and medical treatment of patients in the intensive care unit.
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Application of modern care standards and digital documentation (PDMS).
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Interdisciplinary collaboration with doctors, therapists, and other professionals.
Your Profile:
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Completed training as a registered nurse (m/f/d).
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Experience in intensive care is desirable but not mandatory.
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Teamwork, commitment, and a sense of responsibility.
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Willingness to work in shifts.
Advantages:
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Flexible working hours, including the option of a 4-day workweek.
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Comprehensive training and development opportunities, e.g., specialization in intensive care and anesthesia.
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Attractive additional benefits: company pension scheme, Christmas bonus, job ticket, bike leasing.
- Family-friendly work environment with emergency childcare services.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Job offers Life Sciences
Clinical Data Scientist (m/f/d) - Benelux, Ref. 133
For our client, a biotech company in Scandinavia, we are looking for a:
Clinical Data Scientist (m/f/d)
Reference number: 133
Location: Benelux
Contract type: Full time/Hybrid
Area/department: Not specified
Salary: Not specified
Data is the heartbeat of modern medicine, and your role is to give it a voice. As a Clinical Data Scientist, you bridge the gap between complex raw information and the life-changing therapies of tomorrow. You do not just see numbers; you see the potential to improve patient outcomes and accelerate scientific discovery in an environment where precision is paramount.
How you will make an impact:
In this pivotal role, your expertise ensures that clinical data translates into meaningful medical progress through analytical excellence:
• Oversee the end-to-end clinical data lifecycle for international trials.
• Develop and validate electronic Case Report Forms (eCRFs) and comprehensive data management plans.
• Perform complex data cleaning, transformation, and analysis to ensure the highest levels of data integrity.
• Ensure all datasets strictly comply with international CDISC standards (SDTM and ADaM).
• Collaborate closely with clinicians, biostatisticians, and programmers to drive study success.
• Identify and resolve data discrepancies through rigorous quality control and proactive problem-solving.
• Contribute to the continuous improvement of data science workflows and the implementation of new digital tools.
What you bring to the role:
You combine analytical precision with a passion for the life sciences and a collaborative spirit that thrives in international teams:
• A university degree in Life Sciences, Statistics, Computer Science, or a related quantitative field.
• Proven professional experience in Clinical Data Management or Clinical Data Science within the industry.
• Proficiency in data-driven programming languages such as R, Python, or SAS.
• A solid understanding of ICH-GCP guidelines and global regulatory requirements.
• A strong analytical mindset with the ability to translate complex datasets into actionable insights.
• Excellent communication skills and the ability to act as a bridge between technical and non-technical stakeholders.
• Fluency in English (written and spoken); additional knowledge of Dutch or French is a distinct advantage.
Why you will love working here:
Join a culture that values work-life balance, scientific excellence, and the unique perspective every individual brings to the team:
• A flexible hybrid working model that allows you to balance professional impact with personal life.
• A flat Scandinavian hierarchy that encourages open communication, trust, and individual initiative.
• Dedicated budgets for professional development and continuous learning opportunities.
• A comprehensive benefits package, including a competitive pension scheme and health insurance.
• A modern, inclusive workplace culture rooted in transparency and mutual respect.
• Regular team events and the opportunity to work within a truly international network.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Bioprocess Engineer (m/f/d) - UK, Ref. 132
For our client, a biotech company in the UK, we are looking for a:
Bioprocess Engineer (m/f/d)
Reference number: 132
Location: UK
Contract type: Full time
Area/department: Bioprocessing & Operations
Salary: By agreement
In the world of biotechnology, the journey from a microscopic discovery to a life-saving therapy is paved with engineering excellence. As a Bioprocess Engineer, you are the vital architect of this transition, ensuring that precision and scalability go hand in hand to meet global patient needs. Joining our client’s team in the UK means placing your technical expertise at the forefront of medical innovation, where your dedication directly translates into human health. If you are driven by the challenge of mastering complex biological systems within a collaborative, future-facing environment, this is your next step.
How you will make an impact:
In this pivotal role, you will bridge the gap between laboratory science and commercial reality, driving manufacturing success through your technical leadership:
• Lead the scale-up and optimisation of upstream and downstream manufacturing processes to maximise yields and efficiency.
• Take full responsibility for monitoring and troubleshooting complex bioprocessing equipment and automated systems.
• Collaborate closely with R&D teams to ensure a seamless technology transfer for new therapeutic candidates.
• Manage and execute validation protocols (IQ/OQ/PQ) in strict accordance with cGMP standards.
• Analyse production data to identify trends and implement continuous improvement initiatives (Lean/Six Sigma).
• Maintain meticulous documentation of all processes to satisfy international regulatory requirements and quality audits.
• Provide technical guidance and mentorship to junior staff, fostering a culture of operational excellence.
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What you bring to the role:
Your technical foundation and your passion for quality are what will enable you to excel in our fast-paced, high-stakes manufacturing environment:
• A university degree in Biotechnology, Chemical Engineering, Bioengineering, or a related life sciences discipline.
• Solid professional experience within a biopharmaceutical or biotech manufacturing environment.
• Hands-on expertise with bioreactor systems, fermentation, or protein purification technologies.
• A sound understanding of cGMP guidelines and international quality management systems.
• An analytical mindset with a proactive, solution-oriented approach to technical challenges.
• Excellent communication skills and the ability to work effectively within cross-functional, international teams.
• High levels of personal responsibility, reliability, and a commitment to maintaining the highest standards of safety and quality.
Why you will love working here:
We offer an environment that values your expertise and provides the resources for you to thrive both personally and professionally:
• Attractive remuneration package with a comprehensive company pension scheme.
• Access to industry-leading professional development and subsidised training programmes.
• Private medical insurance and a dedicated health and wellness programme for all employees.
• Flexible working models and modern structures that promote a healthy work-life balance.
• State-of-the-art laboratory and production facilities equipped with the latest bioprocessing technology.
• A vibrant, inclusive company culture with regular team-building events and a strong sense of community.
• Relocation assistance for candidates moving to join our innovative hub in the UK.
How we start our conversation:
voWi Consulting will guide you discreetly and professionally on your path to this position. Are you interested? Then apply either via our "speed application" or simply upload your CV. Naturally, we treat your application documents with absolute confidentiality. We will get back to you promptly.
Quality Manager (m/f/d) – Germany, Ref. 125
Are you a passionate Quality Manager looking for an exciting new professional challenge in Germany?
Then we have just the right opportunity for you!
Our client, a growing, medium-sized pharmaceutical company with a clear focus on quality, knowledge and trust, which distributes phytopharmaceuticals and chemically defined drugs and offers its partners pharmaceutical services in the areas of regulatory affairs, drug safety and quality management is looking for:
A committed Quality Manager (m/f/d) who will take on responsibility together, shape processes and share our values, to strengthen their young team.
Ref.: 125
Position: Quality Manager (m/f/d)
Location: Germany, North Rhine-Westphalia
Contract Type: Full-time
Department: Quality Assurance / Quality Control
Salary: Not specified, please specify your salary expectations.
What you can expect:
- You will maintain and further develop their quality management system (including SOPs, CAPAs, internal audits)
- Your prospects: You will take on the role of the person responsible for wholesale (§ 52a AMG) in the future
- You will work closely with other departments and external partners
- You will be part of a company that values trust, integrity and reliability – not just on paper, but in our daily interactions
What we offer:
- A responsible role in an innovative pharmaceutical company
- An appreciative working environment characterised by respect, team spirit and open communication
- Hybrid working & flexible working hours – because flexibility is not just a word, but a way of life
- Structured induction with individual training
- Opportunities for personal development and active involvement in shaping processes
- An employer who values not only knowledge and quality, but also your ideas and initiative
Ideally, you will have:
- A degree in a pharmaceutical or scientific field (e.g. pharmacy, biology, chemistry, medicine)
- Experience in quality management, ideally also in pharmaceutical quality assurance/control or wholesale
- Confident use of QM systems and very good German (C1) and English skills
- Care, personal responsibility and a structured approach
- Desire to work in a young team with flat hierarchies and fast decision-making processes
Our values – your working environment:
Respect, trust, integrity and flexibility are at the centre of the pharmaceutical company's corporate culture, as is a belief in effective work, the power of knowledge and the reliability of each individual. The company's quality standards are not only required by law but are also a shared promise – to customers and within the team.
If you are interested? Send us your CV. Your data will of course be treated in the strictest confidence.
Medical Device Engineer – UK, Ref. 117
Are you a passionate engineer or scientist looking for an exciting new professional challenge in the medical device field?
Then we have just the right opportunity for you!
For our client, a medical device company in the UK, we are currently seeking a:
Ref.: 117
Position: Medical Device Engineer
Location: UK
Contract type: Full-time
Sector: Medical Technology
Key Responsibilities:
- Hands-on R&D work to improve material formulation for performance and regulatory compliance.
- Design and optimisation of production processes with a focus on quality and efficiency.
- Manufacturing of devices under ISO 13485 standards on a pilot scale.
- Development, refinement, and validation of testing protocols.
- Responsibility for maintenance and qualification of lab equipment.
- Detailed documentation and data management according to strict regulatory guidelines.
- Close collaboration with the technical team and regular reporting on progress.
Qualifications:
- A completed Bachelor’s degree in Chemistry, Biomedical Engineering or Life Sciences.
- Experience in a bio/chemistry lab and with polymer materials.
- Skills in experimental design and data analysis.
- Curiosity and enthusiasm for medical device development.
- Independent working style, reliability, team spirit, commitment, and willingness to learn.
- Strong sense of responsibility, problem-solving skills, and time management.
Benefits:
- Opportunities for professional development and internal career progression.
- Direct collaboration with an experienced, interdisciplinary team in a supportive work environment.
- Flexible working hours (Monday to Friday, flexitime). High visibility of your work and the opportunity to contribute your own ideas.
If you are interested? Send us your CV. Your data will of course be treated in the strictest confidence.
Clinical Trial Manager - Sweden, Ref. 112
We are seeking an experienced Clinical Trial Manager to oversee and coordinate clinical trials for our pharmaceutical client in Sweden. The role will entail managing all aspects of clinical trials across various medical areas, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines. The position offers a hybrid work arrangement, combining remote work with occasional on-site presence.
Ref.: 112
Position: Clinical Trial Manager
Location: Sweden
Contract type: Full-time
Sector: Pharma
Key Responsibilities:
- Develop and manage clinical trial protocols, timelines, and budgets
- Coordinate with cross-functional teams, including investigators, sponsors, and regulatory bodies
- Oversee site selection, initiation, and management
- Ensure compliance with regulatory requirements, GCP, and internal SOPs
- Monitor trial progress and data quality, addressing issues promptly
- Manage and mentor clinical research associates (CRAs) and other trial staff
- Prepare and review clinical trial documentation and reports
- Collaborate with data management teams to ensure data integrity and timely analysis
- Contribute to the development of clinical development plans and strategies
- Represent the company in meetings with investigators, sponsors, and regulatory authorities
Qualifications:
- Bachelor’s degree in Life Sciences, Nursing, or related field; Master’s degree preferred
- Minimum 5 years of experience in clinical research, with at least 3 years in a management role
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements
- Strong project management skills and experience with clinical trial management systems
- Excellent communication and interpersonal skills
- Fluency in English; proficiency in Swedish is a plus
- Certification such as ACRP or SOCRA is highly desirable
Benefits:
- Competitive salary with performance-based bonuses, depending on experience and qualifications
- Flexible work arrangements (remote/hybrid)
- Comprehensive health insurance
- Retirement savings plan
- Professional development opportunities
- Generous paid time off
If you are interested? Send us your CV. Your data will of course be treated in the strictest confidence.
