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This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special.

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📍 United Kingdom

🔍 Clinical Research Organization (CRO)

  • Degree in a numerate discipline preferred or equivalent experience with a minimum of 1 year in finance or accounting.
  • Strong organizational and self-motivation skills with a focus on quality.
  • Excellent written and verbal communication skills in English.
  • Ability to handle multiple tasks and work under pressure.
  • Advanced knowledge of financial software applications and relevant ERP experience.
  • Strong Microsoft Excel skills and proficiency in other MS-Office applications.

  • Prepare and render invoices to sponsors/clients, including services and reimbursements.
  • Assist with billing, accounts receivable reporting, and reconciliations.
  • Reconcile unbilled services and deferred revenue on the balance sheet.
  • Ensure compliance of expenses with internal policies and client requirements.
  • Identify process gaps and help expedite resolutions.
  • Assist with annual audits and statutory tax filings.

Communication SkillsCollaborationMicrosoft ExcelAccountingCompliance

Posted 2024-11-19
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📍 United States of America

🔍 Clinical Research Organization (CRO)

  • Mastery in negotiating complex contract terms with clinical sites and vendors.
  • In-depth understanding of international and local regulatory requirements for clinical trials (e.g., FDA, EMA, ICH-GCP).
  • Ability to explain complex contract terms clearly and concisely.
  • Leadership skills to guide and support junior contract specialists.
  • Ability to collaborate effectively with cross-functional teams, including legal, finance, data protection, and clinical operations.
  • Bachelor's Degree or equivalent in business administration, finance, law, science, or related field.
  • Proficiency with MS Word, Excel, and Outlook.
  • Knowledge of ICH and GCP Guidelines and local country legislation in the sphere of clinical trials.

  • Act as a Subject Matter Expert (SME) on Clinical Trial Agreement processes at country and site level.
  • Preparation, negotiation, and finalization of site contracts and budgets.
  • Manage the Investigator Budget and serve as a key liaison for contract-related communications.
  • Resolve negotiation issues and escalating risks, drive process improvements, contribute to SOP development, and keep templates updated.
  • Liaise and collaborate with Worldwide stakeholders and external stakeholders, such as sites and investigators.
  • Review and finalize Clinical Trial Agreements and associated documents for completeness and accuracy.

LeadershipCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaborationMicrosoft Excel

Posted 2024-11-07
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📍 Brazil, Mexico, Colombia, Chile

🔍 Clinical Research Organization (CRO)

  • Bachelor’s Degree or a Nursing Degree required.
  • 2+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role.
  • 3+ years’ experience as a Clinical Research Associate.
  • Oncology experience required.
  • Excellent interpersonal, oral, and written communication skills in English.
  • Ability to lead and motivate a team remotely.
  • Demonstrate initiative and problem-solving skills.
  • Strong customer focus, ability to interact professionally within a sponsor contact.
  • Proficiency in Microsoft Office, CTMS, and EDC Systems.

  • Provide leadership and direction to clinical site management team members from study start through to closure.
  • Serve as Site Management’s primary point of contact and representative for clinical monitoring and site activities.
  • Manage monitoring deliverables to achieve the study budget and identify Out of Scope Activities.

LeadershipProject ManagementCommunication SkillsCollaborationProblem SolvingMicrosoft OfficeWritten communication

Posted 2024-10-24
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📍 United States, Canada

🔍 Clinical Research Organization (CRO)

  • 7+ years of Clinical Project Management experience, preferably in a CRO setting.
  • University/College degree in Life Science is preferred.
  • Required experience managing radiopharmaceutical studies.
  • Thorough knowledge of project management processes and budget management.
  • Ability to manage multi-office projects and travel as needed.
  • Excellent communication skills and proficiency in Microsoft Office, CTMS, and EDC Systems.

  • Coordinate and manage clinical trials from start-up to closeout activities.
  • Direct technical, financial, and operational aspects to ensure completion of clinical trials.
  • Collaborate with functional area leads to address issues, interpret complex data, and implement solutions.
  • Ensure project deliverables align with customer expectations for time, quality, and cost.

LeadershipProject ManagementProject CoordinationCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-10-22
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📍 France, Germany

🧭 Full-Time

🔍 Clinical research, health sciences

  • BA/BS in business or life sciences.
  • MS or MBA preferred.
  • Clinical Operations background preferred.
  • Extensive knowledge in sales methods and practices.
  • Knowledgeable in the drug development process, preferably in a CRO.
  • Four (4) to six (6) years of experience in Bioanalytical Laboratory, Central Laboratory, Phase I, IIB Clinical Research or CRO industries.
  • At least five (5) years prior sales experience.
  • Fluency in English language – written and oral.

  • Achieve individual revenue and sales objectives through proactive communication and sales for late phase services.
  • Establish connections with biotechnology and pharmaceutical contacts.
  • Identify new leads for Phase II-IV business.
  • Develop strategies for client growth and retention.
  • Aid in project proposal development, including client communication and budget reviews.
  • Coordinate trade show arrangements and ensure activities run smoothly.

LeadershipBusiness DevelopmentPeople ManagementCross-functional Team LeadershipBusiness developmentCommunication SkillsCollaborationOrganizational skillsPresentation skills

Posted 2024-10-21
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📍 United Kingdom

🧭 Full-Time

🔍 Clinical Research

  • MD or OD degree from an accredited medical institution, preferably specializing in the relevant therapeutic area.
  • Minimum of 2 years of experience in medical monitoring or as a study physician.
  • Strong organizational, interpersonal, and communication skills.
  • Knowledge of ICH, GCP, and FDA or EU regulations.
  • Proficiency in MS Office applications and willingness to learn new systems.

  • Work with global teams and sponsors to provide medical expertise and support.
  • Engage from protocol development to regulatory submission process.
  • Provide medical monitoring for clinical studies and train project teams on therapeutic indications.
  • Review study documents and collaborate with pharmacovigilance on Serious Adverse Events.
  • Represent Medical Affairs in meetings and contribute to proposals and feasibility assessments.

Business DevelopmentGCPBusiness developmentCommunication SkillsCollaborationOrganizational skills

Posted 2024-10-21
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📍 United States, Canada

🔍 Clinical Research Organization (CRO)

  • 7+ years' Clinical Project Management experience required within a CRO setting is preferred.
  • Oncology CAR-T experience in a Project Management role is required.
  • University/College degree in Life Science is preferred.
  • Thorough knowledge of project management processes and budget management.
  • Demonstrated experience managing multidisciplinary project teams.
  • Ability to work with little or no supervision.
  • Proficiency in Microsoft Office, CTMS, and EDC Systems.
  • Ability to travel when needed.

  • Responsible for the overall coordination and management of clinical trials from start-up through closeout activities.
  • Directs the technical, financial and operational aspects of the projects to ensure successful completion.
  • Works with functional area leads to identify and evaluate issues, interpret data, and implement solutions.
  • Ensures project deliverables meet customer time, quality, and cost expectations.
  • Collaborates with a dedicated team focused on advancing healthcare in the CGT space.

LeadershipProject ManagementPeople ManagementProject CoordinationCross-functional Team LeadershipCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-10-21
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📍 Poland, Spain, United Kingdom, Romania, Italy, Hungary, Bulgaria, Serbia

🔍 Clinical Research Organization (CRO)

  • 7+ years' Clinical Project Management experience required within a CRO setting.
  • University/College degree in Life Science preferred.
  • Thorough knowledge of project management processes and budget management.
  • Experience in managing multidisciplinary project teams.
  • Excellent communication skills in English and proficiency in relevant software.

  • Responsible for the overall coordination and management of clinical trials.
  • Directs technical, financial, and operational aspects of projects.
  • Works with functional area leads to identify issues and interpret complex data.
  • Ensures project deliverables meet customer's time, quality, and cost expectations.

LeadershipProject ManagementPeople ManagementProject CoordinationCross-functional Team LeadershipOperations ManagementCommunication SkillsAnalytical SkillsCollaborationMicrosoft Office

Posted 2024-10-21
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