Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a
Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a
Senior SAP SD/MM Consultant – S/4HANA Public Cloud – English C1 – LATAM Remote Location: Remote (LATAM) Work Mode: 100% Remote Contract Type: Freelance Language: English C1 + Fluent Spanish (mandatory) Role Description We are looking for
Senior SAP SD/MM Consultant – S/4HANA Public Cloud – English C1 – LATAM Remote Location: Remote (LATAM) Work Mode: 100% Remote Contract Type: Freelance Language: English C1 + Fluent Spanish (mandatory) Role Description We are looking for
At Astek, we are looking for an experienced and globally minded Senior SAP SD Consultant with strong expertise in E-Invoicing solutions and SAP Document and Reporting Compliance (DRC) to join our international team for our pharma
At Astek, we are looking for an experienced and globally minded Senior SAP SD Consultant with strong expertise in E-Invoicing solutions and SAP Document and Reporting Compliance (DRC) to join our international team for our pharma
At Astek, we are looking for an experienced and globally minded Senior SAP SD Consultant with strong expertise in E-Invoicing solutions and SAP Document and Reporting Compliance (DRC) to join our international team for our pharma
MMS Holdings Inc is seeking a Medical Writer to join our remote team in Mexico. Under minimal supervision, you will evaluate literature, write and edit clinical development documents, and manage writing assignments with solid regulatory knowledge. The
MMS Holdings Inc is seeking a full-time Medical Writer to join our data-focused CRO team remotely from Colombia. The role involves evaluating medical literature, drafting clinical development documents, and ensuring regulatory compliance across submission materials. You will