Lediga jobb LINK Medical Research AB i Uppsala

Denna tjänst är ledig på vårt kontor i Uppsala, Stockholm eller Malmö.
Är du intresserad av etiska regler för marknadsföring? Portföljen av kunder som efterfrågar support angående marknadsföringsefterlevnad enligt läkemedelsbranschens etiska regelverk (LER*) ökar.
Vi söker därför efter en positiv och engagerad Marketing Compliance Manager, som vill börja i vårt härliga team av experter inom Regulatory/Compliance.
Som Marketing Compliance Manager kommer du att arbeta i nära samarbete med medlemmar i interna och externa projektteam, med lokala och internationella projekt, och inom en rad olika terapeutiska områden inom läkemedels- och medicinteknisk industri. Som konsult inom LINK Medical Research kommer du att leverera högkvalitativa tjänster i enlighet med våra kunders förväntningar. Du kommer att få möjlighet att utveckla din kompetens efter våra kundbehov och delta i aktiviteter relaterade till affärsutveckling.
Tjänsten kan innebära outsourcing till kunder i Uppsala- Stockholmsområdet alt Malmö-området.
*Läkemedelsbranschens etiska regelverk
Det etiska regelverket LER innehåller bestämmelser för företagens information om läkemedel, samverkan mellan läkemedelsbranschen och intresseorganisationer samt hälso- och sjukvårdspersonal, umgänge med politiker och regler för icke-interventionsstudier.
Kvalifikationer
· Naturvetenskaplig examen på högskole-/universitetsnivå eller liknande utbildning.
· God IT-kompetens
· Flytande i svenska och engelska (skriftligt och muntligt)
· 2+ års erfarenhet av arbete med det etiska regelverket LER
· IMA-certifikat (från LIF-utbildning)
· Tidigare arbete med Veeva Promomats är önskvärt
· Erfarenhet av Regulatory Affairs är önskvärt
Personliga egenskaper:
· God initiativförmåga
· Serviceinriktad med god samarbets- och kommunikationsförmåga
· Noggrann och detaljfokuserad
· Flexibel och ansvarstagande
· Lösnings- och resultatorienterad
· God planerings- och organisationsfärdigheter och förmåga att prioritera
· God förmåga och önskan att uppfylla våra kundlöften: Kvalitet, punktlighet och kommunikation
Ansvar:
· Genomföra projekt/tjänster enligt överenskommelse med projektledare och kund
· Marknadsefterlevnadssupport, t.ex. samråd och råd om nationell lagstiftning och specifika krav
· Granskning av marknadsföringsmaterial enligt den nationella läkemedelskoden (LER)
· Säkerställa kundernas positiva uppfattning om samarbetet med LINK Medical
· Samarbeta nära med det lokala och nordiska Marketing Compliance Team
· Engagera dig aktivt i Compliance-nätverk för att vara en del av att forma miljön och bra branschpraxis
· Bidra till att utveckla ditt kompetensområde inom LINK Medical
· Andra ansvarsområden, såsom uppgifter inom Regulatory, kan ingå i denna tjänst
LINK Medical erbjuder:
En spännande och utmanande position i en europeisk CRO som har en stark lokal närvaro. Företaget fokuserar på samarbete, erfarenhetsutbyte och kontinuerlig utveckling av våra medarbetare i en internationell miljö och värderingar som ärlig och öppen kommunikation är väsentliga. Du kommer att få meningsfulla uppgifter som kräver ett effektivt samarbete mellan industri, regulatoriska och vetenskapliga team samt myndigheter. Förutom en bra arbetsmiljö med engagerade och stödjande kollegor erbjuder vi ett konkurrenskraftigt kompensations- och förmånssystem för alla anställda.
Kontaktinformation
Om du vill veta mer eller har några frågor om tjänsten, vänligen kontakta Charlotte Lavallee, Group Manager, Sverige via telefon; +46 76 105 56 69 eller via e-post; [email protected].
Alla ansökningar behandlas konfidentiellt. Lokala sökande kommer att prioriteras.
Vi lägger stor vikt vid personlig lämplighet.
Goda förutsättningar för balans i livet är viktigt för oss och vi tillämpar flextid och förmånliga villkor gällande bland annat hemarbete och semester. För att främja ett hållbart arbetsliv erbjuder vi också friskvårdsbidrag.
Sista ansökningsdag: 24 september, 2023
Denna rekrytering sker helt genom Link Medicals försorg. Vi undanber oss därför telefonsamtal från rekryteringsföretag och annonsförsäljare. Visa mindre

This position is open at our office in Uppsala, Sweden; Stockholm, Sweden; Malmö, Sweden.
LINK Medical is searching for a Group Manager Clinical Project Management (CPM) with line management of 5-7 CPMs. The work also entails work as CPM (50%). Our company is growing, and the portfolio of cross-functional projects is increasing. The CPM is one of the most exciting and special positions in our company. It takes a special talent to be a successful CPM. This is an extremely special position because you need to have very good knowledge of clinical trials, understand the deliverables of the project, collaborate with your LINK team and also collaborate and get to know what the client needs. You need to be able to communicate and manage many things with high quality and within budget. We offer an international environment and unique team of highly specialized and talented colleagues who work together to creatively solve challenges and deliver high-quality results. We offer competitive salaries, careers development paths, and opportunities to learn and grow.


Responsibilities
Line Management of 5-7 Clinical Project Managers-keep oversight of recourcing, recruitment, training, performance management, development plans and salaries, department budget and processes
Work as Clinical Project Manager (50%): execution of Phase I-IV multinational and medical device trials from initiation until end of the trial. Serve as the primary contact towards the customer, team member and vendors. You are responsible for ensuring that projects run within LINK Medical are completed with high quality and in time, within the budget, and in accordance with the customer’s requests and regulatory requirements.



Desired qualifications
Natural science degree at university level
Previous experience from clinical trials and project management, preferably from a CRO or the pharmaceutical industry
Previous line management experience is meritorious
Since most of our customers are international, good knowledge in English, in both speech and writing, is a requirement



Personal characteristics
Very good cooperative ability and ability to create a good relationship with our customers and staff
Listen, consult others and create a positive atmosphere
You are flexible, structured and service-oriented
Ability to take initiative and quick decisions, act with confidence and work independently



LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given meaningful tasks requiring efficient collaboration between industry, clinical and scientific teams and the authorities. We offer a competitive compensation and benefit scheme for all employees. Visa mindre

We are looking for a Clinical Project Manager. The job is based at LINK Medical Research in Sweden.
Be part of amazing, new, and innovative projects at LINK Medical. We are not just looking for a regular person, the Clinical PM is one of the most exciting and special positions in our company. It takes a special talent to be a successful PM. this is an extremely special position because you need to have very good knowledge of clinical trials, understand the deliverables of the project, collaborate with your LINK team and also collaborate and get to know what the client needs. You need to be able to communicate and manage many things with high quality and within budget. We offer an international environment and unique team of highly specialized and talented colleagues who work together to creatively solve challenges and deliver high-quality results. We offer competitive salaries, careers development paths, and opportunities to learn and grow.


Responsibilities and duties:
Execution of Phase I-IV multinational trials from initiation until end of the trial
As a CPM, you serve as the primary contact towards the customer. The CPM’s daily tasks consist largely of communication (via meetings, e-mail, and telephone) with other team members, vendors, and the sponsor.
You are responsible for ensuring that projects run within LINK Medical are completed with high quality and in time, within the budget, and in accordance with the customer’s requests and regulatory requirements.

Education and competence:
University degree within natural sciences.
Previous experience from clinical trials and project management is merit, preferably from a CRO or the pharmaceutical industry.
Since most of our customers are international, good knowledge in both Swedish and English, in both speech and writing, is a requirement.
Very good cooperative ability and ability to create a good relationship with our customers.
You are flexible, structured and service-oriented.



LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given challenging tasks requiring a good collaboration with both colleagues and customers. We offer a competitive salary, pension, and a benefit scheme for all employees. Visa mindre

This position is based at any of our offices in Sweden (Stockholm, Malmö, Uppsala).
Do you want to join a growing company with a portfolio of cross-functional projects and be part of amazing, new, and innovative projects at LINK Medical?
As a Senior Biostatistician, you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. We offer a variety of stimulating and challenging responsibilities in a friendly team made of statisticians and programmers who focus on collaboration and sharing of experience. We work in an open and flexible environment.
Responsibilities
Responsible for statistical activities within clinical studies (e.g. statistical input to protocols, sample size calculations, generation of randomization lists, writing statistical analysis plans, interpretation of statistical analysis results, producing statistical reports and contributing to clinical study reports)
SAS programming of statistical analyses in clinical studies
SAS programming of analysis datasets in clinical studies
Mentoring of less experienced biostatisticians
Supporting the business development department in bid defense meetings and customer contacts
Development and adaptation of processes within the biometrics department


Desired qualifications
MSc in statistics or mathematical statistics or similar field
Minimum 5 years of experience in statistics within clinical trials
Experience of SAS programming in clinical trials
Fluent in English
Generally good IT skills and use of standard office tools

Helpful but not required
Experience from statistics within oncology
Experience from biostatistical advice for clinical study designs
Knowledge in CDISC standards
Experience from real world evidence projects

Personal characteristics
Service-minded with good collaboration and communication skills
Well organized and structured, able to work both independently and in teams
Team player, flexible, accountable and solution-oriented


LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience, and continuous development of our employees. You will be given meaningful tasks requiring efficient collaboration between industry, clinical and scientific teams, and the authorities. We offer a competitive compensation and benefits scheme for all employees. Visa mindre

Do you want to join a growing company with a portfolio of cross-functional projects?
As a SAS Programmer, you will work in close collaboration with members of internal and external project teams, with local and international projects, and within a range of different therapeutic areas. We offer a variety of stimulating and challenging responsibilities in a friendly team made of statisticians and programmers who focus on collaboration and sharing of experience. We work in an open and flexible environment.
This position is preferably based at our Uppsala or Stockholm office, but we also welcome applicants who wish to be based in our office in Malmö.


Main responsibilities
Support project managers and clients with high quality SAS programming such as, but not limited to, study specific reports, risk-based monitoring reports and metric reports
SAS programming of analysis datasets in clinical studies
SAS programming of tables, listings and figures in clinical studies

Other responsibilities
Project management and coordination of activities related to data management and statistics

Minimum requirements
Natural science or relevant degree at college/university level
Programming skills, preferably SAS
Fluent in English
Generally good IT skills and use of standard office tools

Merits
Experience of SAS programming in clinical trials
Experience in clinical data management and project management
Knowledge in statistics within clinical trials
Knowledge in CDISC standards

Personal characteristics
Service minded with good cooperation and communication skills
Well organized and structured, able to work both independently and in teams
Flexible, accurate and solution oriented

 
LINK Medical offers
LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given meaningful tasks requiring efficient collaboration between industry, clinical and scientific teams and the authorities. We offer a competitive salary, pension and insurance scheme and a bonus scheme for all employees. Visa mindre

We are looking for a Clinical Project Manager. The job is based at LINK Medical Research in Sweden.
Be part of amazing, new, and innovative projects at LINK Medical. We are not just looking for a regular person, the Clinical PM is one of the most exciting and special positions in our company. It takes a special talent to be a successful PM due to the fact that you need to have very good knowledge of clinical trials, understand the deliverables of the project, collaborate with your LINK team and also collaborate and get to know what the client needs. You need to be able to communicate and manage many things with high quality and within budget. We offer an international environment and unique team of highly specialized and talented colleagues who work together to creatively solve challenges and deliver high-quality results. We offer competitive salaries, careers development paths, and opportunities to learn and grow


Responsibilities and duties:
Execution of Phase I-IV multinational trials from initiation until end of the trial
As a CPM, you serve as the primary contact towards the customer. The CPM’s daily tasks consist largely of communication (via meetings, e-mail, and telephone) with other team members, vendors and the sponsor.
You are responsible for ensuring that projects run within LINK Medical are completed with high quality and in time, within the budget, and in accordance with the customer’s requests and regulatory requirements.



Education and competence:
University degree within natural sciences.
Previous experience from clinical trials and project management is merit, preferably from a CRO or the pharmaceutical industry.
Since most of our customers are international, good knowledge in both Swedish and English, in both speech and writing, is a requirement.
Very good cooperative ability and ability to create a good relationship with our customers.
You are flexible, structured and service-oriented.



LINK Medical offer:
LINK Medical offers an exciting and challenging position in a European CRO that has a strong local presence. The company focuses on collaboration, sharing of experience and continuous development of our employees. You will be given challenging tasks requiring a good collaboration with both colleagues and customers. We offer a competitive salary, pension, and insurance scheme and a bonus scheme for all employees. Visa mindre

Till vårat kontor i Uppsala.LINK Medical söker en Löneadministratör på deltid. I tjänsten ingår förutom ren lönekörning, all personaladministration, allt från framtagande av anställningsavtal till underhåll av personalregister. Vi har idag en annan lösning för administration av löner och personaluppgifter vilket ger möjlighet för rätt person att utforma nya rutiner efter eget huvud.Önskade kvalifikationer:Erfarenhet av att självständigt hantera löneadministration.Grundläggande erfarenhet av personaladministrationGrundläggande erfarenhet av regelverk kring anställning och lön och förmåner.Noggrann, flexibel och självgåendeAnsvar:All lönehantering för bolagets 3 kontor i sverige (totalt ca 80 personer) vilket innebär:Löpande lönekörningarLöpande uppdatering av personalregister, inklusive löner och förmånerAdministration av Pensioner och försäkringarKontaktperson för personalrelaterad myndighetsrapportering, tex försäkringskassan och SCBKontroll av reseräkningar Visa mindre