!*Associate Director, Clinical Development - Internal Medicine - Spain!*
Location:
Anywhere in SpainStart date:
ASAP
Job Description
We're currently working with a held biopharmaceutical company focused on developing innovative therapies for unmet medical needs. They specialize in areas such as
rare diseases ,
ophthalmology, and
biotechnology, and are known for pioneering treatments.
Their approach blends
advanced R&D, including AI-powered drug discovery platforms, with a strong commitment to scientific collaboration. They also engage in the production of medical devices, supplements, and over-the-counter products, maintaining a broad therapeutic portfolio across multiple disciplines.
The Associate Director of Clinical Development is instrumental in the planning, execution, and analysis of clinical trials. This role collaborates closely with cross-functional teams to drive the progression of our pipeline. We’re seeking a candidate with a strong foundation in clinical research and drug development, coupled with a sharp ability to transform scientific insights into effective clinical strategies
Key Responsibilities:
Long Description:
Contribute to the design and execution of clinical development programs, ensuring alignment with regulatory and business objectives.Support protocol development, clinical study reports, investigator brochures, and other clinical documents.Collaborate with cross-functional teams, including biostatistics, regulatory, medical affairs, and clinical operations, to ensure high-quality trial execution.Analyze and interpret clinical trial data to inform decision-making and regulatory submissions.Monitor emerging scientific and competitive developments in the therapeutic area to inform clinical strategy.Provide scientific expertise to support interactions with investigators, regulatory agencies, and key opinion leaders.Assist in the preparation of regulatory documents, including INDs, NDAs, and clinical sections of regulatory filings.
Requirements:
MD, specialising in Internal Medicine.Looking for someone with experience across Phases I-III.
If this role isn’t suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated! Planet Pharma offers a competitive referral scheme so you will be rewarded for your help!
About Planet Pharma
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including:
Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.