Senior Medical Monitor / Associate Medical Director

REQUIREMENTS

To be accountable for medical support on clinical studies conducted by the Medical team including clinical interpretation of data and to ensure clinical trials are conducted such that patients safety is protected and that the clinical trial data are reliable.

To act as Medical Monitor for assigned trials and participate in all stages of the clinical trial development process including: feasibility assessments, protocol design, case report form design, investigational site selection, ongoing medical support and management of adverse events and serious adverse events, and generation of medical/patient narratives and clinical study reports.

To assume assigned activities and support the team within Pharmacovigilance, including the review of CIOMS narratives, and to identify and communicate emergent safety aspects and trends to the clinical project teams and client.

To provide therapeutic area support at all levels within the company, including the provision of required internal training, and review of study/bid proposals. To maintain knowledge of trends and changes of importance in the medical management of indications relevant to company projects.

To ensure highest ethical standards in the conduct of clinical trials and to support the Medical Department in establishing Best Practices for the department, including the development of standard operating procedures and company processes. To maintain knowledge of relevant regulations and guidelines and disseminate this to clinical project teams as applicable.

QUALIFICATIONS

• MD / Medical Doctor / Physician
• 5+ years’ experience within CRO or Pharmaceuticals
• 3+ years’ experience as a Medical Monitor
• Dynamic, customer facing individual who excels in fast paced environments

 LOCATION

London, United Kingdom (offering some flexibility to work from home)

DURATION

Permanent

SALARY

Competitive benefits package

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 recognised 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.

www.planet-pharma.com

TO APPLY

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0)203 868 8607 or e-mail on schapple@planet-pharma.co.uk

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!