Last updated: 2025-05-22

17 Business Development And Sales jobs in Remote - Kingdom of Spain.

Hiring now: Sr Dir Global Program Tea @ Astrazenec, Regulatory Mgr Sr Regulat @ Precision , Team Mgr Veeva Rim Profes @ Veeva Syst, Sr Medical Writer @ Parexel, Site Contracts Spec Sr Si @ Syneos Hea, Contract Negotiator Fsp E @ Iqvia, Clinical Ops Mgr Spain @ Betterhelp, Sr Feasibility Associatef @ Pfm.Explore more at at kaamvaam.com

šŸ”„ Skills

clinical trials (8) project management (6) compliance (5) Regulatory Affairs (4) drug development (3) biopharmaceutical (3) leadership (2) Regulatory strategy (2) Clinical trials (2) Regulatory submissions (2)

šŸ“ Locations

Kingdom of Spain (17)

Astrazeneca

Skills & Focus: program ownership, global development strategy, oncology, drug development, clinical plans, project management, regulatory influence, collaborative, leadership, biopharmaceutical
About the Company: AstraZeneca is a global pharmaceutical company focused on the discovery, development, and commercialization of prescription medicines. They are committed to im…
Experience: Ten (10)+ years in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology
Type: Full-time

Precision For Medicine

Skills & Focus: Regulatory strategy, Clinical trials, Regulatory submissions, Compliance, Project management, Regulatory Authorities, Drug development, Clinical Research Organisation, ICH, Quality initiatives
Experience: 5 to 7 years Regulatory experience

Veeva Systems

Skills & Focus: Team Manager, Veeva RIM, Professional Services, implementation, consultants, coaching, life sciences, regulatory processes, project management, data management
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: 8+ years of hands-on software implementation experience at a software vendor or consulting firm within the life sciences R&D or healthcare space, 2+ years experience of managing professional services consultants
Benefits: Employees are shareholders; Veeva Giving program supports charitable causes; strong stance against non-compete agreemen…

Parexel

Senior Medical Writer Kingdom of Spain
Skills & Focus: medical writing, clinical research, biopharmaceutical, drug development, medical content, medical documents, clinical trials, regulatory submissions, technical writing, medical communications
About the Company: Parexel is a global clinical research organization that provides a range of services to help biopharmaceutical companies develop new drugs and medical treatmen…

Precision For Medicine

Skills & Focus: clinical trials, Oncology, Project Management, CRO, GCP, clinical development, budget management, client relationship, cross-functional team, medical terminology
About the Company: Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading ope…
Experience: 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
Type: Full-time

Parexel

Skills & Focus: Clinical Trials, Investigator Contracts, Spain, FSP, Remote Work, Biopharmaceutical, Regulatory Affairs, Patient Experience, Consulting, Medical Writing
About the Company: Parexel is a global biopharmaceutical services organization that provides solutions in consulting, clinical research, and commercialization. The company specia…
Type: Full-time

Syneos Health

Skills & Focus: clinical, contracts, clinical trial, management, negotiating, regulatory, startup, phases, assurance, compliance
About the Company: Syneos HealthĀ® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success in clinical development, medical affai…
Experience: High level of contracts management experience

Precision For Medicine

Skills & Focus: Regulatory strategy, Clinical trials, Regulatory submissions, Orphan designations, Clinical development, Regulatory guidance, Regulatory Affairs, Drug development, Clinical Research, Compliance
About the Company: Precision for Medicine is a precision medicine Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medici…
Experience: 5 years for Manager level and 7 years for Senior Manager level
Skills & Focus: regulatory strategy, clinical trials, regulatory submissions, Regulatory Authorities, clinical development, orphan designations, regulatory guidance, project management, submission targets, drug development
About the Company: Precision for Medicine is focused on helping life sciences organizations to accelerate drug development by providing regulatory and clinical trial expertise ta…
Experience: 5 years Regulatory experience required for the Manager level and 7 years Regulatory experience required for the Senior Manager Regulatory level

Iqvia

Skills & Focus: contract negotiation, clinical research, contract management, budget templates, proposal development, clinical trials, investigator grants, compliance, financial contracting, team collaboration
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 2 to 5 years relevant sponsor or clinical research organization clinical site contracting experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Parexel

Skills & Focus: Regulatory Affairs, CMC, Pharmaceutical, Biologics, Quality Control, Submission Strategies, Market Expansions, Risk Management, Collaboration, Technical Documentation
About the Company: Parexel is a global biopharmaceutical services company that provides expertise in regulatory affairs, clinical research, and other related fields to help bring…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, supportive and inclusive environment, opportunities for career growth.

Iqvia

Skills & Focus: clinical trials, project management, communication, problem solving, leadership, planning, time management, financial management, vendor management, stakeholder engagement
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 5 years of prior relevant experience including > 1 years project management experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Betterhelp

Skills & Focus: clinical operations, mental health, remote teamwork, customer-centric, data-driven, compliance, quality improvement, clinical care, public speaking, therapist engagement
About the Company: BetterHelp is on a mission to remove the traditional barriers to therapy and make mental health care more accessible to everyone. Founded in 2013, we are now t…
Experience: 7+ years independently providing direct clinical care
Type: Contractor
Benefits: The chance to build something that changes lives - an awesome community of co-workers.

Parexel

Skills & Focus: Regulatory Affairs, project management, clinical trials, client relationships, compliance, project execution, budget management, resource planning, cross-functional teams, therapeutic areas
About the Company: Parexel is a global biopharmaceutical services organization that provides a broad range of expertise to support the development and market access of innovative…
Experience: extensive experience in Regulatory Affairs, PMP or equivalent certification preferred

Iqvia

Study Start Up Lead Kingdom of Spain
Skills & Focus: site activation, clinical trials, regulatory compliance, project management, biotechnology, clinical practice guidelines, study initiation, budget planning, contract negotiation, regulatory intelligence
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 7 years relevant experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Pfm

Skills & Focus: feasibility analysis, site identification, clinical trials, pre-award, post-award, site outreach, feasibility projects, biotech, pharma, biopharmaceutical
Experience: 5 years

Iqvia

Skills & Focus: clinical trial management, global coordination, vendor management, stakeholder engagement, compliance, GCP, trial execution, budget monitoring, data management, issue resolution
About the Company: IQVIA is a leading global provider of information, innovative technology solutions, and contract research services focused on the healthcare industry.
Experience: 6-8 years clinical trial management experience in the pharmaceutical industry or CRO.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.