PPD are currently looking for CTMs to join our team.
This exciting and unique role could take you to the next step of
your career within Clinical Research. The role coordinates all aspects of clinical activities
on an international basis. This includes the day to day management and leadership of a team of
Clinical Management members which are allocated to a project on a Country basis. You will work
in partnership with the Project Manager to ensure the necessary training, tracking and quality
systems are in place for the clinical management team, and be primarily responsible for the
clinical deliverables of the Project within agreed timelines and budget. Clinical Team Managers
provide contact and support to the project sponsor for all clinical aspects.
We are seeking high performing individuals who enjoy a fast-paced
environment and have had Clinical Project Management experience and exposure to international
studies, involving the coordination of CRA/PA/RSM-L/RSM-C across different countries. With your
excellent written and oral English skills you will have exceptional interpersonal and problem
solving skills, with the ability to lead CRAs in different countries. You will also have
proficient working knowledge of GCP and experience in several medical / therapeutic areas. You
must be comfortable working in a matrix management system and have the ability to motivate,
mentor and integrate international teams.
Sounds like you? We are seeking highly motivated and skilled
applicants who will want to share in our continued growth in the international market place. If
you succeed we can offer you the opportunity to grow into enhanced roles within the department
and also have examples of Clinical Team Managers who have moved into project management or
management of CRAs. We will consider field based applicants depending on your experience
level.
Must have:
·
Bachelor's degree or licensed certified health
care training or equivalent combination of education and experience
·
Previous oversight management activities in excess
of 6 months e.g. as STM/ PM or one year of proven delegated management
activities:
o
Coordination of local clinical team members based
in more than one country other than the own
o
Training and presenting at study
meetings
o
Oversight activities for systems, e.g. CTMS, EDC,
ePIP
o
Communication with sponsors
o
Facilitating/chairing team
teleconferences
o
MVR report review
·
Clinical research experience in all phases of
study life cycle, including start up, interim and close out
·
Willingness to cross-region and in region travel
according to the project needs
·
Be competent in use of written and oral English
language
·
Valid Driver's License
·
Valid Passport
Knowledge, Skills and
Abilities:
·
Superior organizational
skills
·
Strategic thinking skills
·
Demonstrated performance management
abilities
·
Extensive monitoring
experience
·
Excellent judgment and decision making
skills
·
Excellent interpersonal skills and problem solving
ability
·
Highly effective verbal and written communication
and presentation skills
·
Ability to motivate and integrate teams and
teach/mentor team members
·
Expert knowledge of relevant regulations e.g.
ICH/GCP, FDA guidelines, etc.
Please submit your CV in
English.
This is an ongoing search. Suitable
candidates will be contacted accordingly.
Preference will be given to Employees from the
Designated Groups in line with the provisions of the Employment Act No. 55 of 1998 (and any
amendments thereto), PPD’S INTERNAL recruitment policy and the employment equity
plan.
*LI-ST2
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