Associate Clinical Research Manager

Job Description

With support of other CRMs and/or TA-Head/CRD this role is accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations policies and procedures quality standards and adverse event reporting requirements internally and externally.

The a CRM could be responsible for a particular study for a country or a cluster.

Responsibilities include but are not limited to:

Main Point of Contact (POC) for assigned protocols and link between Country Operations
and clinical trial team (CTT).
Responsible for project management of the assigned studies:
pro-actively plans drives and tracks execution and performance of
deliverables/timelines/results to meet country commitments from feasibility and site
selection recruitment execution and close out.
Accountable for performance for assigned protocols in a country in compliance with
ICH/GCP and country regulations policies and procedures quality
standards and adverse event reporting requirements internally and externally.
o Reviews Monitoring Visits Reports and escalates performance issues and training
needs to CRA-Manager and/or functional vendor and internal management as
needed.
o Performs Quality control visits as required.
Leads local study teams to high performance: trains in the protocol other local roles closely
collaborates with and supports CRAs as protocol expert and coordinates activities across the
different local country roles ensuring a strong collaboration (including the CTCs CRAs and
COMs).
Responsible for creating and executing a local risk management plan for assigned studies.
Ensures compliance with CTMS eTMF and other key systems in assigned studies.
Escalates as needed different challenges and issues to TA-Head/CRD/CCQM and or CTT
(as appropriate).
Identifies and shares best practices.
Responsible for collaboration with functional outsourcing vendors investigators other
external partners in assigned studies.
As a customer-facing role this position will build business relationships and represent
the company with investigators.
Supports local and regional strategy development consistent with longterm corporate needs
in conjunction with CRD TA-Head and Regional Operations.
Collaborates internally with HQ functions regional and local operations EU Clinical
Development Pharmacovigilance Regulatory Affairs Global Medical and Scientific Affairs
to align on key issues/decisions across the trials. Consult with Human Health as needed.

Skills:

Knowledge in Project Management and/or site management.
Strong organizational skills with demonstrated success in related role or discipline
required.
Requires ability to make decisions independently and oversee important activities
relevant to clinical research activities according to predetermined global policies and
commitments with the support oversight and supervision of the TA-Head or CRD
Requires understanding of local regulatory environment.
Scientific and clinical research knowledge is required.
Understanding of clinical trial planning management and metrics is essential as well
as the ability to focus on multiple deliverables and protocols simultaneously.
Ability to function as a key link between Country Operations and Clinical Trial

Teams
Communicates effectively and builds a collaboration spirit in a remote/virtual environment
and across countries cultures and functions.
Ability to manage processes (and controls) productivity quality and project delivery.
Proficiency in written and spoken English and local language. The incumbent must be
competent and effective in written and verbal communication.
Strategic thinking.
Ability to work efficiently in a remote and virtual environment.
Aptitude for building leadership skills that enable and drive alignment with the goals
purpose and mission of the company Global Clinical Development
(GCD) and GCTO.
Ability to identify problems conflicts and opportunities early analyses and prepare
mitigation plans and drive conflict resolution is critical.

Required to negotiate skillfully in tough situations with both internal and external
groups;settle differences with minimum disruption. Examples of common problems
include: 1) low patient recruitment 2) inadequate staff to meet business needs 3)
performance or compliance issues and 5) resolution of conflictive situations.
Understand cultural diversity.
Strong diplomatic and empathic skills to effectively build and maintain professional
relationships with investigators and other stakeholders.

Qualification & Experience:

4 years of experience in clinical research
Bachelor degree in Science (or comparable)
CRA experience preferred

Required Skills:

Preferred Skills:

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Employee Status:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

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