What are the responsibilities and job description for the Clinical Research Associate position at Galderma S.A.?
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.
We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.
At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.
Job Title : Clinical Research Associate
Job Location : Carlsbad
Responsibilities :
- Clinical trial design in partnership with Director of Clinical Research and the Clinical team.
- Coordinate with other departments as necessary for meeting clinical trial and other R&D initiative timelines.
- Ensure alignment with regulatory standards, including GCP, GMP, and all other applicable regulatory authorities and guidelines.
- Assists with the development and approval of clinical trial documents.
- Conduct scheduling, recruitment, pre-screening and enrollment activities for in-house clinical studies in a Clinical Research Coordinator capacity.
- Ensure the effective execution of in-house clinical trials through maintaining accurate clinical supply inventory.
- Coordination with clinical sites during study start up to ensure delegated staff trainings on devices, cameras, and other instruments for aesthetic studies in accordance with the study protocol.
- Coordination with clinical sites in accordance with HIPAA and privacy laws to ensure appropriate storage and organization of raw data and images for all clinical studies.
- Work with vendors to ensure timely calibration and maintenance of all Sponsor owned clinical devices and equipment and assist with the procurement of new devices, equipment and supportive materials.
- Cross-functional collaboration, working closely with the formulations, operations, and marketing teams to ensure clinical materials align with company goals.
- Build positive relationships with clinical trial investigators and their research team.
- Coordinate and oversee other key research studies / activities as requested by the Director of Research.
- Coordinate the delivery and logistics of clinical trial related materials in collaboration with the clinical team.
- Ability to create compelling, results-driven clinical Before & After content for a range of channels including digital, print, and in-person marketing materials to help substantiate product claims.
Requirements :
Physical Requirements :
