Jobs at ClinChoice

You will be responsible for selling CRO full services, including lead generation, opportunity assessment, and account management. You'll build relationships with key decision-makers and exceed revenue targets. Join a global CRO focused on quality and collaboration.

You will drive business growth by generating leads, assessing opportunities, and managing key client accounts in the life sciences sector. Your work directly supports the company's expansion and helps deliver impactful clinical research solutions.

You will ensure local safety activities comply with regulations and company policies, manage case quality and regulatory submissions, and maintain key performance indicators for a global CRO's client.

In this role, you will drive growth by identifying and pursuing new business opportunities, building relationships with key decision-makers, and selling CRO full services. You'll develop account plans, refine the sales approach, and work to exceed revenue targets while contributing to a collaborative team culture.

You will manage local safety activities for a pharmaceutical client, ensuring compliance with regulations and global standards. You'll perform quality checks on safety reports, track submissions, and maintain KPIs while working part-time from the office and remotely.

You will ensure regulatory data compliance across databases, execute activities such as label preparation and system updates, and support submissions and approvals of market licenses. This 12-month contract role offers the opportunity to work with a global CRO while supporting a single sponsor, balancing multiple activities in a high-trust environment.

You will manage clinical study activities across multiple sites within one or more projects, focusing on medical devices. You'll oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.

You will manage clinical study activities across multiple sites, focusing on medical devices. You'll oversee site performance, conduct company-initiated studies, and ensure quality through site visits and monitoring, working directly with a single sponsor while benefiting from the support of a global CRO.

Join ClinChoice's talent community to be notified when a suitable position becomes available that matches your experience and skillset. You can be part of making a difference in peoples' lives and experience a fulfilling career.

You will handle case processing activities including intake, triage, data entry, and quality review of adverse event reports from various sources. You will also conduct follow-up queries and ensure regulatory compliance in a remote, contract role supporting pharmacovigilance operations.

You will ensure proper submissions and approvals for market licenses, including new registrations, changes, and renewals, while supporting regional teams and interacting with government agencies. This role is a 12-month contract with a global CRO, offering the security of a large organization with direct sponsor engagement.

You will work directly with a sponsor as part of a global CRO, supporting clinical trial programming and submission deliverables. Your work ensures high-quality, compliant statistical outputs for drug development programs.

You will manage clinical study activities across multiple sites for medical device studies, oversee site performance, and ensure high-quality deliverables through site visits and monitoring. This role offers the stability and career growth of a global CRO while working directly with leading pharmaceutical companies in Germany.

You will perform medical review of individual case safety reports (ICSRs) across multiple therapeutic areas, ensuring quality compliance and adherence to regulatory timelines. You will also provide medical guidance, participate in process improvements, and assist in training and mentoring case processing personnel.

You'll lead **programming activities** for clinical studies, developing **TFL deliverables** from SAS programs. This role supports **regulatory submissions** and offers the stability of a global CRO with the focus of a single sponsor.

You'll provide **statistical leadership** for oncology clinical development programs across Phase I–III trials, leading SAPs and regulatory submissions. You'll collaborate with cross-functional teams and contribute to **regulatory interactions** with FDA/EMA. This client-facing role offers the stability of a global CRO with the focus of a single sponsor.

You'll **lead analytical efforts** for a high-profile sponsor at a global CRO, developing **patient cohorts** and validating key variables. Your work will drive **real-world evidence research** across diverse therapeutic areas.

You'll provide **statistical leadership** for respiratory and immunology studies, working on **protocol development and analysis plans**. Your work will directly impact clinical trial readouts for a top pharmaceutical client. This role offers the stability of a global CRO with the focus of a single sponsor.

You'll serve as the **primary statistical lead** for respiratory and immunology studies, providing oversight from protocol development through reporting. You will **ensure data integrity and accuracy** in analyses and deliverables. This role offers the stability of a global CRO with the focus of a single sponsor assignment.

You'll work directly with a single sponsor as a **Senior Statistical Programmer Consultant** at a global CRO, developing and validating SAS programs for **clinical trial data analysis**. You'll create datasets, tables, and listings while collaborating with cross-functional teams to ensure **submission-ready deliverables**.

You'll lead **statistical strategy** for clinical trials across therapeutic areas at a **global CRO**. You'll provide statistical support for Phase I–IV trials, regulatory submissions, and cross-functional collaboration. This permanent role offers the stability of a large organization with diverse sponsor exposure.

You'll lead statistical strategy for clinical trials in **immunology** and other therapeutic areas. You'll author **Statistical Analysis Plans** and ensure regulatory compliance. This role combines sponsor exposure with global CRO career opportunities.

You'll develop and execute **CMC regulatory strategies** for global product filings, supporting post-approval activities and change controls. You'll partner cross-functionally to ensure compliance with **FDA and Health Canada requirements**.

You'll execute data screening and collection for **systematic literature reviews** supporting medical device regulatory documents. Your work directly impacts **Clinical Evaluation Reports** and **Post-Market Surveillance** activities. Join a global CRO with a **collaborative one-team culture**.

You'll **lead statistical activities** for clinical trials in Immunology or other therapeutic areas, acting as the lead statistician on assigned studies. You'll author and review key documents like **Statistical Analysis Plans (SAPs)** and collaborate with cross-functional teams. This role offers the chance to **work remotely** for a global CRO with a strong quality-driven culture.

You'll lead **statistical programming deliverables** for a **Respiratory & Immunology sponsor** while enjoying the stability of a global CRO. Your work will directly support clinical trial data reporting and regulatory submissions.

You'll provide statistical leadership for **Real-World Evidence (RWE)** and **medical affairs** activities, designing and analyzing observational studies to support post-marketing and payer evidence. You'll collaborate closely with cross-functional teams including Medical, HEOR, and Commercial to generate insights that drive publication strategies. This **fully remote** contract role offers the security of a global CRO with the focus of a single sponsor.

You'll lead cross-functional teams and manage complex clinical trials for **pharma and biotech clients**, ensuring delivery aligned with regulatory standards. You'll drive **oncology and respiratory studies** while overseeing budgets and timelines. This role offers **permanent remote flexibility** with a global CRO.

You'll join ClinChoice as a trainee in statistical data programming, working on clinical trial data. You'll contribute to data analysis and reporting using high-level computing languages. **This role offers hands-on experience** in the **pharmaceutical/biotech industry**.

You'll be responsible for the execution, oversight, and delivery of **clinical studies** across a diverse client portfolio. Your core impact will be managing **complex oncology and hematology trials** while ensuring study tracking, vendor management, and site activities run smoothly. This permanent remote role stands out for its **global CRO environment** with a quality-driven culture.

You'll partner with Clinical Operations leadership to support **global clinical trials** across multiple indications. Your core impact will be driving study delivery and operational success for a **Phase III CNS study**. This hands-on role offers significant visibility and impact within a fast-growing biotech sponsor.

You'll prepare and maintain **SOPs and policies** aligned with regulatory standards for a **clinical research organization**. Your work ensures audit readiness and strengthens quality systems. This role offers exposure to **global QMS improvements** and cross-functional collaboration.

You'll lead **statistical programming deliverables** for oncology clinical trials, working directly with a sponsor through a global CRO. You'll ensure high-quality, compliant programming outputs and contribute to best practices. This role offers the stability of a large CRO with direct client engagement.

You'll coordinate and compile data for **Periodic Safety Update Reports** at a **global CRO serving pharma and biotech**. You'll ensure on-time completion by managing stakeholder communication and schedules. **This role offers hands-on regulatory writing experience** in a collaborative team.

You'll lead **statistical programming** for clinical trials using **R and SAS**, working directly for a sponsor with a global CRO's support. Your work will drive data analysis and reporting for regulatory submissions. This role offers a permanent position with the security of a large organization and the variety of a sponsor-focused model.

You'll lead statistical programming for clinical trials at a global CRO. You'll **program and validate datasets** and **oversee CRO deliverables** to ensure high-quality submissions. This permanent role offers **the stability of a sponsor and career growth of a CRO**.

You'll drive **full clinical operations service growth** by securing new clients and expanding services within existing accounts. You'll manage the **full sales lifecycle** from prospecting to closing complex, high-value deals. This role offers **hybrid or remote work** depending on your location.

You'll provide statistical support for Medical Affairs studies, including observational and real-world evidence research. You'll partner with cross-functional teams to ensure high-quality data analysis and interpretation. This role offers the stability of a global CRO with the autonomy of a client-facing position.

You'll join a global CRO to manage clinical trial data for a single sponsor, ensuring accuracy and regulatory compliance. You'll oversee end-to-end data management activities and collaborate with cross-functional teams. This permanent role offers career stability with the resources of a large organization.

You'll lead statistical strategy and analysis for clinical trials in the Vaccines and Infectious Diseases therapeutic area. Your work will directly impact **regulatory submissions** to FDA and EMA. You'll collaborate with cross-functional teams and ensure **CDISC-compliant deliverables**.

You'll lead **statistical programming** activities for **clinical trials**, developing SDTM and ADaM datasets and producing Tables, Listings, and Graphs for FDA submissions. Your work will directly support regulatory filings and ensure data integrity.

You'll drive growth across **pharmacovigilance, regulatory, and medical affairs services** by securing new clients and expanding existing accounts. You'll manage the full sales lifecycle from prospecting to closing **complex, high-value deals**. This role offers **flexible remote or hybrid work**.

You'll support **biometric access management** and **CCTV monitoring** at a clinical research organization. Your work ensures a secure and efficient workplace for clinical trial operations. This role offers exposure to **vendor coordination** and cross-functional admin tasks.

You'll lead strategic oversight of aggregate reporting, risk management, and surveillance operations for a global CRO serving top pharma and biotech clients. Your core impact is ensuring regulatory compliance and quality across all safety reports. This role offers the chance to shape a growing pharmacovigilance practice and drive **innovation in safety surveillance**.

You'll lead **statistical programming deliveries** for oncology clinical trials at a global CRO, working directly with a sponsor. You'll ensure **high-quality CDISC-compliant outputs** and contribute to best practices. This role offers the security of a large organization with the autonomy of a consultant.

You'll join the Scientific Computing Technology group to build open-source tools, R packages, and computing systems for clinical programming. Your core impact will be developing CDISC-compliant SDTM and ADaM datasets and **contributing to the pharmaverse**. This role blends hands-on clinical deliverables with contributions to internal tooling.

You'll join the **Statistical Programming** team to support **clinical trial data analysis** using SAS/R. You will complete a structured training program and contribute to producing tables, listings, and figures for low-complexity studies. This role offers hands-on experience in a global CRO environment.

You'll lead **statistical programming efforts** for a **CVRM (Cardiovascular, Renal, Metabolism) team** at a top pharmaceutical company. Your work will directly support **regulatory submissions** and clinical trial reporting. This is a remote contract role with a global CRO.

You'll lead **statistical programming deliveries** for clinical studies in a **client-facing role** at a global CRO. Your work directly supports oncology trials, ensuring high-quality data and compliance with regulatory standards.

You'll lead **cross-functional teams** overseeing complex clinical trials for a **global CRO**. Your work ensures delivery aligns with contractual commitments and regulatory requirements. This permanent remote role lets you drive **hematology/oncology studies**.