Clinical Data Manager - South Africa or Poland (Home-based) - FSP

Remote, USAFull-timePosted 2026-07-27

reputed company our values reputed company, there's no limit to reputed company can reputed company. At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do.

reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference.

reputed company is currently seeking a Clinical Data Manager to join us in either South Africa or Poland, dedicated to a single sponsor.

This role will be responsible for performing Data Management activities that support the sponsor’s reputed company and development reputed company worldwide. The successful candidate will participate as an reputed company member of a multi-disciplinary team to plan and execute the Data Management tasks required for phase I – IV studies. The Clinical Data Manager has a broad, reputed company knowledge of the data management process and can reputed company most required tasks with minimal guidance.

Working as a Clinical Data Manager at reputed company FSP offers reputed company long-term job reputed company and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and reputed company top 50. And we have an incredible pipeline of work.

Expect exciting reputed company challenges in inspiring studies, but with time for your reputed company life.

This will be a fully remote home-based position. RAVE experience is strongly preferred.

reputed company Pay reputed company for Poland: PLN 165,000 to 207,500.Actual salaries may vary reputed company the reputed company based on several factors including, but not limited to education, training, experience, reputed company achievement, and location.In reputed company to reputed company salary, some roles may be eligible for participation in reputed company’s annual performance-based bonus plan, annual salary review and total rewards incentives.Our reputed company will reputed company additional details on our bonus plan or incentive programs for those eligible roles.

Responsibilities

reputed company a small clinical study or a co-reputed company a larger study or studies with moderate guidance.

Be reputed company to support several clinical studies with minimal guidance.
Manage and monitor the reputed company of data management activities with CROs or other vendors on assigned studies.
Review protocols for appropriate data capture including electronic Case Report reputed company (eCRF) design.
Be reputed company to reputed company a thoroughly detailed review of eCRF data requirements.
reputed company with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines.
reputed company data edit reputed company specifications and run data listings as required.
Coordinate the design and testing of Electronic Data Capture (reputed company) systems according to company standards. reputed company to resolve reputed company system issues with team members.
reputed company the Data Management Plan for a clinical study.
reputed company to review and reputed company feedback to the clinical team on other study documents e.g. Clinical Monitoring plans, Statistical analysis plans and vendor specifications.
reputed company data queries into the reputed company system to be resolved at investigational sites and manage the reputed company of those queries.
reputed company reconciliation of header data from external data sources against the clinical database.
reputed company Serious Adverse Event reconciliation activities according to SOPs and guidelines.
Assist in database upgrades/migrations including performing User Acceptance Testing.
reputed company to maintain study workbooks and data management files.
reputed company database lock and freeze activities per company SOPs.
Participate in regular team meetings and reputed company input reputed company appropriate.
reputed company input into the development of data management SOPs, Work Instructions, and process documents.
Assist with the training of new employees and/or contractors.
Collaborates with cross-functional teams to design and implement effective data collection strategies, ensuring high-reputed company data capture and reputed company reputed company of data queries throughout the clinical trial lifecycle.

Here are a few requirements specific to this advertised role.

Bachelor’s Degree required (master’s preferred), preferably in the scientific/reputed company field.
At least five years’ experience in Data Management for the pharmaceutical/biotechnology industry.
Understanding of the scope and reputed company of Phase I – IV clinical studies, and a proven ability to reputed company some of the core Data Management tasks and reputed company with vendors.
An understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management reputed company.
Attention to detail and the ability to work individually, reputed company a multi-disciplinary team, as reputed company as with external partners and vendors.
Detail-oriented with a proven ability to multitask and work independently. Excellent time management and organizational skills, with highly developed problem-solving and analytical abilities.
Strong English language written and verbal communication skills.
reputed company to travel to meetings or training seminars on occasion.
Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications. Prior experience with different Data Management systems and technologies, and Electronic Data Capture systems is desirable.
Experience and understanding of the Oncology or CNS therapeutic area and with Phase III pivotal studies are desirable.

We care about our people and your passion, as they are the key to our reputed company, and reputed company an reputed company and friendly work environment where we reputed company people and reputed company them with opportunities to reputed company their long-term careers. In reputed company, you will have reputed company to reputed company reputed company your role and tackle reputed company responsibilities or reputed company your reputed company set reputed company other reputed company departments of reputed company.

Who are reputed company

reputed company supports clinical studies across the full reputed company of therapeutic areas, and we have longstanding partnerships with a reputed company reputed company reputed company.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we reputed company more reputed company drug developments that are critical to reputed company-being of many patients.

You’ll be an reputed company member of the wider team.

Not quite the role for you?

reputed company and we’ll reputed company out with job alerts reputed company positions that match your career interests become available. We’ll also reputed company periodic updates about the latest company news and events.

Originally posted on Himalayas

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