21 Jobs für Clinical Drug Consultant
Stellenangebote Clinical Drug Consultant Jobs
Job am 03.07.2025 bei Jobleads gefunden
• Kassel, Hessen
Führungs-/ Leitungspositionen
Discovery Life Sciences is a global market leader in biospecimen solutions and laboratory services, offering an extensive range of products and services to support
drug discovery and development. With a [...]
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[...] network of laboratories and offices across the United States and internationally, we are committed to advancing scientific research and improving health care outcomes. We are dedicated to accelerating the discovery and development of new therapies and diagnostics by providing the highest quality biospecimens, in vitro [. .. ] teams in assay development and validation which includes semiquantitative as well as quantitative assays Support/ consult our project management and business development team as well as our clients Evaluation of clinical trial specimens Act as a trainer for external pathologists within our post approval services for the interpretation/ scoring of novel biomarkers Preparation of publications/ posters in collaboration with our customers Position Qualifications (Education, Skills, Experience) : Board certification (German board certification preferred) Additional training in Cytology Experience in hematopathology and/[. .. ] on oncology and immunology Excellent knowledge in IHC, m IF, FISH, RNA in situ hybridization to support the assay development team as well as to act as an experienced reader and consultant for customers in clinical trials. Experience in digital imaging applications and the evaluation of biomarkers via digital image analysis software Teamplayer Willingness to work in a GCLP environment Compensation and Benefits: Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total [. .. ]
Job gestern bei Jobleads gefunden
Senior Analyst, Site Contracts and Budgets Germany, Poland, Portugal or UK FSP
• Berlin
When our values align theres no limit to what we can achieve. At Parexel we all share the same goal to improve the worlds health. From
clinical trials to regulatory [...]
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[...] consulting and market access every clinical development solution we provide is underpinned by a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work [. .. ] German and English is essential. An advanced ability to speak and read Polish is also preferred. Responsibilities Negotiate and maintain Clinical Trials Agreements (CTA) , site budgets, Confidential Disclosure Agreements, Consultant Agreements and other applicable contracts. Oversee CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols. Ensure compliance of contracts with Fair Market Value (FMV) principles and guidelines. Track contract progress, complete required followups [. .. ] and regulatory compliance issues. Strong interest in learning more about contracts and budgeting in support of sponsor clinical trials. Working knowledge of clinical trial functions including clinical operations, regulatory and drug safety. Ability to prioritize and manage multiple tasks simultaneously. Fluent in spoken and written German and English (essential) . Advanced spoken and written Polish skills (preferred) . Turkish, Portuguese or Russian language skills are desirable alternatives to Polish language skills. About Parexel Parexel supports clinical studies across the full range [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Beratungs-/ Consultingtätigkeiten
[. .. ] among the first 25 applicants Direct message the job poster from R D Partners Empowering consultancies, biotech, and pharma companies to scale highperforming HTA/ RWE teams with [...]
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[...] strategic recruitment solutions. Consultant Shape the future of clinical trials by driving Patient Reported Outcomes strategies that meet global standards and deliver realworld impact. R D Partners is seeking a skilled PRO Consultant to provide expertise in Patient Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment [. .. ] Proven track record of successful application of PROs with external stakeholders such as FDA, EMA, and HTAs. Advanced knowledge of PRO methods, instruments, and their integration into clinical studies during drug development. For more information, please contact Seb Rose. If you are interested in applying to this exciting opportunity, then please click Apply or to speak to one of our specialists visit the Contact Us page. R D Partners is a leading life sciences recruiter focused on finding exceptional people and [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Scientific Informatics Business Analyst
• München, Bayern
Vacancy Scientific Informatics Business Analyst Location Munich Hours Full-time The
Consultant will support strategic projects primarily for pharmaceutical and Biotech clients. The Consultant will gather business requirements, analyse customer needs [...]
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[...] and gaps to propose solutions for the desired state. He or she will interface with business users and client managers in conjunction with the internal Zifo support team. Core Responsibilities As [. .. ] the activities of peers, and have demonstrated the ability to gain the trust of customers. Thorough understanding in one or more of the following areas of the bio/ pharmaceutical industry Drug discovery and development processes Clinical trial design and data management Laboratory workflows Chemical biologics materials management Sample management Robotic systems integration and qualification Operations KPI and metrics tracking. Be knowledgeable about relevant Regulations and standards that govern the development of technical solutions such as GLP, GMP, 21 CFR Part11, Part210, Part820 regulations. Technical Skills Be [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Bern
Beratungs-/ Consultingtätigkeiten
[. .. ] Day in the Life Would you like to work for a rapidly growing international healthcare company and actively contribute to improving patients quality of life? Do you [...]
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[...] bring the experience, clinical mindset and technical expertise required for a Senior Technical Consultant role? If yes, we look forward to receiving your application and welcoming you into our recruitment process. We are currently looking for a Senior Technical Consultant Neuromodulation responsible for sales and support activities within Central Switzerland. In this position, you will actively shape and optimize customeroriented processes with a strong [. .. ] Accounts, 15 internal administrative and operational activities. Within the Neuromodulation business, you will be responsible for our therapies: DBS (Deep Brain Stimulation) , SCS (Spinal Cord Stimulation) , TDD (Targeted Drug Delivery) . Responsibilities Monitor and support surgical procedures in the field of neuromodulation on a regular basis, support programming of implants, device instruction and patient followup care in selected clinics, provide highlevel technical and clinical expertise to physicians and medical staff. Plan and coordinate dedicated customer support and implement strategic [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Solution Consultant-Post Acute
Beratungs-/ Consultingtätigkeiten
[. .. ] evolves. We continuously strive to advance our Netsmart technologies and offerings beyond the EHR by embracing new technology trends that empower healthcare professionals to provide the best [...]
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[...] possible care. Solution Consultant As a Solution Consultant at Netsmart, you will play a pivotal role in showcasing the value of our solutions and the impact they make for the clients our prospects serve. Your daytoday activities will include kickoff calls to prepare for upcoming demos, collaborating with team members, and conducting discovery calls [. .. ] Netsmart solutions at industry events, trade shows, client meetings and Netsmarts annual health conference meeting Review responses as a part of bid submissions or requests for proposals (RFPs) ; contribute clinical, financial and local workflow expertise as applicable, and share key RFP feedback with solution presenters Maintain appropriate knowledge base for industries served to facilitate ongoing product development and product offerings to market Qualifications Bachelors degree or equivalent relevant work experience At least 3 years of software presales experience demonstrating solution [. .. ] committed to maintaining a drugfree workplace in accordance with applicable federal law. Pursuant to Netsmart policy, all postoffer candidates are required to successfully complete a preemployment background check, including a drug screen, which is provided at Netsmarts sole expense. In the event a candidate tests positive for a controlled substance, Netsmart will rescind the offer of employment unless the individual can provide proof of valid prescription to Netsmarts third party screening provider. If you are located in a state which grants [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Managing
Consultant-Regulatory Affairs Quality Cpl Life Sciences Job Title: Senior Manager, Regulatory Labelling Location: Germany, Fully Remote Salary: Competitive Salary + Excellent Benefits Employee Type: Permanent As a Senior [...]
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[...] Manager, Regulatory Labelling, you will take leadership on everything related to Regulatory Labelling. This includes inputting from a regulatory labelling perspective on developing and established drug programs and being accountable for driving global labelling strategies. This is a challenging opportunity to demonstrate your knowledge in managing regulatory processes and supporting cross-functional teams with end-to-end labelling processes. Responsibilities: Support end-to-end labelling processes including driving labelling strategies for both development programs and established [. .. ] Experience: University Degree in a scientific degree. Experienced in the following: CCDS, PIL, USPI, Target label profiles. 5+ years of experience in drug development especially in labelling, product package coordination, clinical supplies/ packaging, supply chain regulatory affairs, or quality. Good working knowledge of key labeling regulations/ guidance and past experience in label development. The ability to research and create comparator labeling documents. Electronic document management systems use and/or electronic submission experience. Solid understanding of requirements for tracking of labeling updates. [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Physician Senior Consultant at Ambulance Services-Role based in Doha Qatar
• Berlin
Beratungs-/ Consultingtätigkeiten
Physician Senior
Consultant at Ambulance Services Role based in Doha, Qatar 2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive [...]
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[...] features. We are in search of candidates who possess experience in clinical and/or community settings, ideally with a certification in General Practice (Family Medicine) . The purpose of this role is the most senior doctor (apart from the Department Chair and/or Section Head) who practices in a specific specialty and has oversight responsibility for his team of Consultants and junior [. .. ] specialization. Participates in health education programs through orientation and scientific presentations. Participates in scheduling of on-call duties and provides on-call services. Participates in the assessment and updating of drug, medical supply and equipment needs. Writes, completes and approves medical reports for patients. Provides guidance and counsel to other departments when requested. Completes and maintains his set of clinical privileges Complies with Revalidation guidelines and standards Acquires SCH License to practice and maintains it while working for HMC Performs other [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
Sabbaticals
[. .. ] will work cross-functionally and globally to embed sustainable access approaches across the product lifecycle. You will shape national HTA submissions, develop evidence-driven payer value propositions, and translate [...]
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[...] complex clinical and economic data into strategic outcomes. This role will also offer exciting proximity to Modernas digital ambitions, with opportunities to work closely with real-world data and explore synergies with generative AI tools in evidence generation and access storytelling. Heres What Youll Do Your key responsibilities will be: Lead the [. .. ] real-world datasets into compelling payer value stories and clear evidence frameworks. Coordinate cross-functional teams (Market Access, HEOR, Medical, Commercial, external experts) for strategy execution. Act as an internal consultant to align local market insights with global product and platform plans. The key Moderna Mindsets youll need to succeed in the role: We digitize everywhere possible using the power of code to maximize our impact on patients. In this role, the ability to interface with large datasets, claims-based systems, [. .. ] join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work #J-18808-Ljbffr 72357105 [. .. ]
Job am 08.12.2025 bei Jobleads gefunden
Executive Director, Oncology Early Clinical Development Lead
• Zug
Führungs-/ Leitungspositionen
Executive Director, Oncology Early
Clinical Development Lead Join to apply for the Executive Director, Oncology Early Clinical Development Lead role at GSK. GSK aims to positively impact the health [...]
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[...] of 2.5billion people by the end of the decade, focusing on vaccines and medicines that address patients needs with the highest probability of success. Position [. .. ] presentations, and manuscripts for accuracy and compliance. Lead preparation of clinical sections of regulatory filings (IND, study reports, NDA, annual reports, etc. ) . Provide clinical support for investigator and consultant meetings (e. g. , investigator meetings, advisory boards) . Present study results and translational insights to senior management, scientific advisory boards, regulatory agencies, and other stakeholders. Integrate input from research, clinical, medical, scientific, commercial, regulatory, and manufacturing disciplines to ensure alignment and execution of translational research initiatives. Build and maintain [. .. ] in Oncology. Pharmaceutical or relevant scientific/ medical/ clinical experience in Oncology focusing on earlyphase trials (FIH and POC) and translational research. Experience with Oncology treatment guidelines, clinical development process, and drug approval process in major regions. Prior experience developing and driving translational strategy: biomarker, companion diagnostic, PK/ PD modeling and simulation. Preferred Qualifications MD preferred. Board certification or eligibility in oncology. Experience in the gastrointestinal therapeutic area highly preferred. Indepth knowledge of GCP, ICH, FDA, EMEA, NICE, and other regulations. Broad [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Beratungs-/ Consultingtätigkeiten Abgeschlossenes Studium
Firmenwagen Jobticket
# # # Job Title Technical
Consultant Healthcare
Clinical Integration Insights (m/w/d) DACH # # # Job Description Du bist Teil eines dynamischen Teams von Application Consultants, Technical [...]
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[...] Consultants, Solution Architects und Project Managers. Gemeinsam unterstützt und begleitet ihr unsere Kunden der DACH-Region im Rahmen von anspruchsvollen technischen Projekten in der Intensiv- und Anästhesiepflege. Du hast [. .. ] require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/ Vets and maintains a drug-free workplace. #J-18808-Ljbffr 71921994 [. .. ]
Job am 05.12.2025 bei Jobleads gefunden
Associate Director, Pharmacometrics
Führungs-/ Leitungspositionen
Overview Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional
drug discovery and development. Its clients include more than 2, 000 biopharmaceutical companies, academic institutions [...]
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[...] and regulatory agencies across 62 countries. At Certara, we accelerate medicines to patients by partnering with life science innovators. In the past 6 years, over 90 of companies that received new drug approvals by the FDA [. .. ] end platform with biosimulation, regulatory science, and market access solutions combined with our strong team of scientists and subject matter experts enable our clients to have informed decision-making, reduced clinical trial burden, higher R D productivity, improved patient outcomes and increased patient access to medicines, and accelerated regulatory approval. Informed decision-making reduced clinical trial burden Higher R D productivity Improved patient outcomes increased patient access to medicines Accelerated regulatory approval Certara is a global team that nurtures a diverse [. .. ] Responsibilities Support projects for Certaras clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands-on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in [. .. ]
Job am 04.12.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
Senior Principal
Consultant (Medical) at Bio Talent, part of The IN Group Bio Talent are delighted to partner with a rapidly growing biotech client, dedicated to transforming cancer treatment, [...]
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[...] currently hiring for a Global Head of Pharmacovigilance. This is a strategic leadership role responsible for guiding safety strategy, ensuring compliance, and driving successful trial conduct for company assets across all stages of development. The role will direct safety strategy, operations, and regulatory compliance for oncology drug products across clinical development and commercialisation phases. It is central to ensuring safe, compliant, and successful oncology drug development and maximising patient safety from clinical trials to postmarketing surveillance. This position will report to the Chief Medical Officer and may work on a hybrid basis from the company office in Germany or remotely. [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
Sr. Principal Consultant, Regulatory Strategy and Advisory
• München, Bayern
Beratungs-/ Consultingtätigkeiten
Sr. Principal
Consultant, Regulatory Strategy and Advisory Sr. Principal Consultant, Regulatory Strategy and Advisory 1 month ago Be among the first 25 applicants All candidates should have a passion [...]
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[...] for helping our clients navigate transformational change; We are looking for smart, self-driven, high-energy people with top-notch communication skills, intellectual curiosity. [. .. ] and agile delivery experienced Role Summary, Core Expectations In depth knowledge of Pharma Regulatory Operations and Regulatory IT Systems aligned to core Functional and Technical competencies Expert in Regulatory and Clinical area with ability to drive futuristic IT solutions and experience in client facing and agency thought leadership Understanding and knowledge of processes related to health authority submissions, content authoring, labeling, lifecycle management of CMC, regulatory intelligence, and country-specific regulatory requirements-keenly aware of industry trends, needs and business requirements [. .. ] outcomes Technical Credentials: Should have masters degree in a Life Science, Medical or Related discipline. Masters in Business Administration would be an added advantage. Minimum 12-15 years experience in Drug development, Regulatory, Clinical Operation and Medical Devices. Deep understanding of RIM systems i. e. , Veeva Vault, PARAXEL/ LIQUENT In Sight, CSC Regulatory Tracker, Aris Global Register, Open Text, Share Point, Documentum, First Doc/ First Point, Next Docs, CARA, Extedo e CTD Manager, Trackwise, or other regulatory information management systems Submission [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
Overview Associate Business
Consultant-Life Sciences R D and Quality Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. [...]
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[...] As one of the fastest-growing Saa S companies in history, we surpassed 2B in revenue in our last fiscal year with extensive growth [. .. ] data, and consulting. We deliver unique value to this industry through excellent business consulting services powered by Veevas industry-leading software and data. Our R D and Quality teams accelerate drug development across the entire R D value chain-Clinical, Regulatory, Safety, and Quality. We optimize and unify digital operations for our customers to deliver therapies more efficiently, while ensuring patient safety. Learn more about our teams impact and thought leadership through our Resource Hub (see R D Strategy) . We hire Associate Business Consultants across our different teams. If [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Bauingenieur:in als Senior Projektleiter:in für Umbauten 80100
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
Flexible Arbeitszeiten Work-Life-Balance
[. .. ] Lead, RLT Senior Project Manager IT and Digitalisation Technical Project Manager HVAC, Cleanroom, EMS, ALC Manager Global Business Excellence--Temporary position Muttenz, Basel-Country, Switzerland 1 year ago Global [...]
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[...] Drug Regulatory Affairs Project Leader (6602) Associate Director, Technical Project Leader Drug Substance Senior Project Manager: Public Infrastructure Finance for Municipal Development Permanent contract Analytical Project Leader Senior/ Principal Scientist Lead, Real World Sciences Application Strategy m/f/d Drug Product Project Leader Oral Dosage Forms (80-100) Consultant Technology Transfer-Fill Finish Team Lead MES PI Competence Center (f/m/d) , 80-100 Senior Global Business Process Specialist Financial Accounting Senior Clinical Operations Manager-6575 Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 65375776 [. .. ]
Job am 11.09.2025 bei Jobleads gefunden
Associate Business Consultant-Life Sciences R D and Quality
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
Associate Business
Consultant-Life Sciences R D and Quality Join to apply for the Associate Business Consultant-Life Sciences R D and Quality role at Veeva Systems. Overview Veeva Systems is [...]
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[...] a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the [. .. ] on customer-facing engagements to create high-impact business solutions. We deliver value to the Life Sciences industry through software, data, and consulting. Our R D and Quality teams accelerate drug development across the entire R D value chain Clinical, Regulatory, Safety, and Quality. We optimize digital operations for our customers to deliver therapies more efficiently while ensuring patient safety. Learn more about our teams impact through our Resource Hub (see R D Strategy) . We hire Associate Business Consultants across our different teams. If multiple teams interest you, apply [. .. ]
Job am 27.08.2025 bei Jobleads gefunden
Director, Pharmacometrics
• Basel, Basel- Stadt
Führungs-/ Leitungspositionen
[. .. ] and the people that need them most. Innovation and creativity are highly valued, and everyone is given the opportunity for training and continuous development. Our portfolio spans [...]
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[...] the discovery, preclinical, clinical and post-marketing phases of drug development, working with 1, 200 commercial companies, 250 academic institutions, and numerous regulatory agencies. In the past 6 years, over 90 of companies that received new drug approvals by the FDA used our software or services. Our integrated and proprietary end-to-end platform with biosimulation, regulatory science, and market [. .. ] interests. Support projects for Certaras clients by working in teams with other Associates, senior expert modelers, and drug development consultants. Hands on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in [. .. ]
Job vor 5 Tagen bei Neuvoo.com gefunden
R D Partners
PRO Consultant
• Stuttgart
Beratungs-/ Consultingtätigkeiten
Shape the future of
clinical trials by driving Patient-Reported Outcomes strategies that meet global standards and deliver real-world impact. R D Partners is seeking a skilled PRO
Consultant [...]
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[...] to provide expertise in Patient-Reported Outcomes (PRO) within the pharmaceutical industry. This role focuses on designing and refining PRO strategies for clinical trials, ensuring alignment with strategic objectives and regulatory requirements. Please note that to be considered for this role you must have the right to work in this [. .. ] Proven track record of successful application of PROs with external stakeholders such as FDA, EMA, and HTAs. Advanced knowledge of PRO methods, instruments, and their integration into clinical studies during drug development. For more information, please contact Seb Rose. If you are interested in applying to this exciting opportunity, then please click Apply or to speak to one of our specialists visit the Contact Us page. R D Partners is a leading life sciences recruiter focused on finding exceptional people and [. .. ]
Job vor 10 Tagen bei Neuvoo gefunden
Zifo RnD Solutions
Scientific Informatics Business Analyst
• Munich, Bavaria
Vacancy Scientific Informatics Business Analyst Location Munich Hours Full-time The
Consultant will support strategic projects primarily for pharmaceutical and Biotech clients. The Consultant will gather business requirements, analyse customer [...]
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[...] needs and gaps to propose solutions for the desired state. He or she will interface with business users and client managers in conjunction with the internal Zifo support team. Core Responsibilities: As [. .. ] the activities of peers, and have demonstrated the ability to gain the trust of customers. Thorough understanding in one or more of the following areas of the bio/ pharmaceutical industry: Drug discovery and development processes Clinical trial design and data management Laboratory workflows Chemical biologics materials management Sample management Robotic systems integration and qualification Operations KPI and metrics tracking. Be knowledgeable about relevant Regulations and standards that govern the development of technical solutions such as GLP, GMP, 21 CFR Part 11, Part 210, Part 820 regulations. [. .. ]
Job am 20.10.2025 bei Job-Consult gefunden
PhD- Jobs. NET
Specialist Adult Psychiatry
• Schweden/ sonstiges/ Europa
[. .. ] supervision of younger colleagues is included as a natural part of the work and participation in the units medical development specialists perform the most physician specific tasks [...]
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[...] such as diagnostics drug treatment and the establishment of a care treatment plan together with the team on the other hand psychotherapies are conducted by psychotherapists with other basic professionals dutywork is included in the service both daily and evening night duties you also need knowledge to replace your staff when vacation illness etc [. .. ] participating in the development of this we also wish you to have an interest in adhd treatment and substitution treatment for opiate addiction number of vacancies education specialist education psychiatry clinical experience what kind of treatments patients do you expect the doctor to have experience with years of experience all of the vacancies involve working with most of the psychiatric diagnoses why a broad background is a plus special knowledge and skills or special interests that are important to the job [. .. ] as a specialist your role will be to back up the residents when you get a delegation to deal with emergency care issues which usually happens when you get a consultant employment your duty will instead be a backup doctor to apply please send your cv mentioning reference lr at info phd jobs net contact person vitaly pryadka tel web http www phd jobs net gesundheits sozialwesen sonstiges europa medizin pharma sozialwesen vollzeit 66556414 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Consultant pro Jahr?
Als Clinical Drug Consultant verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Consultant Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 21 offene Stellenanzeigen für Clinical Drug Consultant Jobs.
In welchen Bundesländern werden die meisten Clinical Drug Consultant Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Consultant Jobs werden derzeit in Bayern (3 Jobs), Berlin (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Consultant Jobs?
Clinical Drug Consultant Jobs gehören zum Berufsfeld Pharmazie.
