Medical Monitor - Oncologist required!

Location
Europe
Salary
Competitive package
Posted
02 Apr 2021
Closes
02 May 2021
Ref
SAMAMD24
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

SUMMARY

Our client is a midsize organization specialized in complex Oncology indications with clinical trials running in Phase I-IV. The role of Medical Monitor is a wonderful opportunity for an experienced Physician/Oncologist to join a successful and growing business offering long-term career opportunities and visibility within a small team structure.

RESPONSIBILITIES

  • Acts as Medical Monitor for more complex trials.
  • Supports the Medical Director in resolving general department CAPAs, escalations and cascading any audit findings to the study team during monthly department meetings.
  • Generation of protocol and synopsis writing with sponsor and Technical Writing team.
  • Review Clinical Study report and provides feedback to the Medical and Technical Writing team.
  • Participates in all stages of the Clinical Trial Development process, e.g., feasibility assessments, protocol design, case report form design, investigational site selection, medical monitoring plan development, ongoing medical support, management of AE's and SAE's, and involvement in trial-related meetings.
  • Responds to study specific audit queries and supports in the resolution of the audit findings
  • Generates Medical and Patient narratives and safety update reports.
  • Provide therapeutic area support throughout the organisation, including the provision of required internal training and review of study/bid proposals.
  • Supports the study team in reviewing audit findings that require medical input and communicates to the Head of the Department to apply corrective and preventive actions.
  • Support Clinical Development/Senior Clinical Development physician in their assigned studies when required.

QUALIFICATIONS

  • Physician / Medical Degree (MBBS, MD, Doctor of Medicine etc.)
  • Experience in medical monitoring, review of patient, laboratory, and safety within a clinical research environment
  • Experience in business development activities, including feasibility and strategic advice for proposal development and bid-defence meetings
  • Excellent organisation and time management skills. Ability to effectively manage any changes to priorities/deadlines
  • Experience in Regulatory and sponsor audit and resolving CAPAs.
  • Experience in Pharmacovigilance process, including medical review.
  • Professional communication and presentation skills
  • Strong computer skills including but not limited to the knowledge of electronic data capturing systems and MS-Office products such as Excel and Word

DURATION

Permanent / full-time

SALARY

Attractive package

LOCATION

Homebased anywhere in EU/UK

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

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